Cyclic amine CCR3 antagonist

ABSTRACT

A medicine containing, as an active ingredient, a cyclic amine derivative represented by the following formula (I), 
                         
a pharmaceutically acceptable acid addition salt thereof or a pharmaceutically acceptable C 1  to C 6  alkyl addition salt thereof. The medicine has an action for treating or preventing diseases in which CCR3 participates, such as asthma and allergic rhinitis.

This application is a 371 of PCT/JP00/05260, filed Aug. 4, 2000, which claims the priority of Japan application Ser. No. 11/220,864, filed Aug. 4, 1999.

TECHNICAL FIELD

The present invention relates to a CCR3 antagonist which can be expected to have effects as a remedies and/or a prophylactics against diseases, for whose progress and maintenance the increase and tissue infiltration of eosinophils, basophils, activated T-cells and the like play main rolls, for example, allergic diseases such as asthma, allergic rhinitis, atopic dermatitis, urticaria, contact dermatitis and allergic conjunctivitis, inflammatory bowel diseases such as ulcerative colitis and Crohn disease, eosinophilia, eosinophilic gastroenteritis, eosinophilic enteropathy, eosinophilic fasciitis, eosinophilic granuloma, eosinophilic pustular folliculitis, eosinophilic pneumonia, eosinophilic leukemia and the like, or AIDS (acquired immunodeficiency syndrome) caused by the infection of HIV (human immunodeficiency virus).

BACKGROUND ART

In recent years, a concept that the essential pathosis of allergic diseases such as asthma is chronic inflammation has been established, and the accumulation of eosinophils at an inflammatory region is especially thought to be one of the principal characteristics of the diseases (refer to, for example, Busse, W. W. J. Allergy Clin. Immunol., 1998, 102, S17-S22; Takao Fujisawa, Gendai Iryo, 1999, 31, 1297, and so on). For example, when an antibody against intercellular adhesion molecule-1 (ICAM-1) was administered into a simian asthmatic model, the accumulation of eosinophils was inhibited, and the manifestation of a late asthmatic response was controlled. Thereby, the importance of the eosinophils in allergic diseases was strongly suggested (Wegner, C. D. et al., Science, 1990, 247, 456).

Eotaxin was identified as a specific chemotactic factor causing the accumulation/chemotaxis of eosinophil (refer to, for example, Jose, P. J., et. al., J. Exp. Med., 1994, 179, 881; Garcia-Zepda, E. A. et al., Nature Med., 1996, 2, 449; Ponath, P. D. et al., J. Clin. Invest., 1996, 97, 604; Kitaura, M. et al., J. Biol. Chem., 1996, 271, 7725, and so on). Further, it was elucidated that eotaxin bound to a CCR3 receptor expressed on eosinophil to display the action, and it is also known that chemotactic factors such as RANTES (abbreviation of regulated upon activation normal T-cell expressed and secreted), MCP-2 (abbreviation of monocyte chemoattractant protein-2), MCP-3 (abbreviation of monocyte chemoattractant protein-3), and MCP-4 (abbreviation of monocyte chemoattractant protein-4) can exhibit the same actions as that of the eotaxin through CCR3, although the action potencies of the chemotactic factors are weaker than that of the eotaxin (refer to, for example, Kitaura, M. et al., J. Biol. Chem., 1996, 271, 7725; Daugherty, B. L. et al., J. Exp. Med., 1996, 183, 2349; Panath, P. D. et al., J. Exp. Med., 1996, 183, 2437; Hiath, H. et at., J. Clin. Invest., 1997, 99, 178; Patel, V. P. et al., J. Exp. Med., 1997, 185, 1163; Forssmann, U. et al., J. Exp. Med. 185, 2171, 1997, and so on).

Not only an action for causing chemotaxis but also actions related to the activation of eosinophils, such as the enhancement in the expression of adhesion molecule receptor (CD11b) (refer to, for example, Tenscher, K. et al., Blood, 1996, 88, 3195, and so on), the stimulation in the production of active oxygen (refer to, for example, Elsner, J. et al., Eur. J. Immunol., 1996, 26, 1919, and so on), the stimulation in the release of EDN (abbreviation of eosinophil-derived neurotoxin) [refer to El-Shazly, et al., Int. Arch. Allergy Immunol., 1998, 117 (suppl. 1), 55], have been reported as the actions of the eotaxin on the eosinophils. It has also been reported that eotaxin has an action for stimulating the release of eosinophils and their precursor cells from bone marrow into blood (refer to, for example, Palframan, R. T. et al., Blood, 1998, 91, 2240, and so on).

Many reports show that eotaxin and CCR3 play important roles on allergic diseases such as asthma. For example, the inhibition of eosinophil infiltration with an anti-eotaxin antibody in a mouse asthma model (refer to Gonzalo, J.-A. et al., J. Clin. Invest., 1996, 98, 2332), the inhibition of eosinophil infiltration with an anti-eotaxin antiserum in a mouse dermal allergy model (refer to Teixeira, M. M. et al., J. Clin. Invest., 1997, 100, 1657), the inhibition in the formation of pulmonary granuloma with an anti-eotaxin antibody in a mouse model (refer to Ruth., J. H. et al., J. Immunol., 1998, 161, 4276), the inhibition of eosinophil infiltration in an asthma model and an interstitial keratitis model using eotaxin gene-deficient mice, respectively, (refer to Rothenberg, M. E. et al., J. Exp. Med., 1997, 185, 785), the increase in the expression of eotaxin and CCR3 in the bronchus of an asthmatic patient at a genetic level and a protein level in comparison with a healthy subject (refer to Ying, S. et al., Eur. J. Immunol., 1997, 27, 3507), and the increase in the expression of eotaxin in the nasal subepithelium tissue of a chronic sinusitis patient (refer to Am. J. Respir. Cell Mol. Biol., 1997, 17, 683), have been reported.

Additionally, since it has been reported that eotaxin is expressed in large amounts in the inflammatory regions of Crohn disease and ulcerative colitis which is an inflammatory large bowel disease (refer to Garcia-Zepda E. A. et al., Nature Med., 1996, 2, 449), it can be understood that the eotaxin also plays important roles on the diseases.

From these data, it is strongly suggested that the eotaxin accumulates and activates the eosinophils in the lesion regions through CCR3 and thereby deeply participates in the initiation progression and maintenance of diseases in which the deep participation of the eosinophils in the progresses of the lesions can be supposed, for example, allergic diseases such as asthma, allergic rhinitis, atopic dermatitis, urticaria, contact dermatitis, and allergic conjunctivitis, inflammatory bowel diseases such as ulcerative colitis and Crohn disease, eosinophilia, eosinophilic gastroenteritis, eosinophilic enteropathy, eosinophilic fasciitis, eosinophilic granuloma, eosinophilic pustular folliculitis, eosinophilic pneumonia and eosinophilic leukemia.

Further, since they have been reported that CCR3 receptors reveal not only on eosinophils but also on basophils and Th2 lymphocytes and that the increase in the intracellular calcium ion concentrations of the cells and the chemotaxis of the cells are caused by the eotaxin, the eotaxin and the CCR3 are supposed to have relations with the initiation progression and maintenance of the diseases in which the cells participate, such as allergic diseases, also by the accumulation and activation of the cells (refer to, for example, Sallusto, F. et al., Science, 1997, 277, 2005; Gerber, B. O. et al., Current Biol., 1997, 7, 836; Sallusto, F. et at., J. Exp. Med., 1998, 187, 875; Uguccioni, M. et al., J. Clin. Invest., 1997, 100, 1137; Yamada, H. et al., Biochem Biophys. Res. Commun., 1997, 231, 365; and so on).

Thereby, a compound for inhibiting the binding of eotaxin to the CCR3, namely, a CCR3 antagonist, is supposed to be useful as a medicine for treating and/or preventing diseases such as allergic diseases and inflammatory intestinal diseases by inhibiting the action of a CCR3 ligand represented by the eotaxin on a target cell, but a medicine having such the action is now not known.

In addition, since it has been reported that HIV-1 (human immunodeficiency virus-1) utilizes CCR3 on the infection of a host cell, a CCR3 antagonist is supposed to be useful for a medicine for treating or preventing AIDS (acquired immunodeficiency syndrome) caused by the infection of the HIV (refer to, for example, Choe, H. et at., Cell, 1996, 85, 1135; Doranz, B. J. et al., Cell, 1996, 85, 1149).

Recently, it has been reported that xanthene-9-carboxamide derivatives (refer to WO 9804554), piperazine or piperidine derivatives (refer to EP 903349; WO 0029377; WO 0031033; WO 0035449; WO 0035451; WO 0035452; WO 0035453; WO 0035454; WO 0035876; WO 0035877), pyrrolidine derivatives (refer to WO 0031032), phenylalanine derivatives (refer to WO 9955324; WO 9955330; WO 0004003; WO 0027800; WO 0027835; WO 0027843), and other low molecular compounds (refer to WO 9802151) have antagonistic activities to CCR3 receptors. However, these compounds are different from the compounds used in the present invention. And, the compounds used in the present invention are the same as the compounds mentioned in WO 9925686, but it is not known that these compounds have antagonistic activities to CCR3 receptors.

DISCLOSURE OF THE INVENTION

Thereby, the object of the present invention is to provide low molecular compounds, which have activities to inhibit that the ligand of CCR3, such as eotaxin, binds to the CCR3 on a target cell.

Another object of the present invention is to provide a method for treating and/or preventing, with a CCR3 antagonist, such a disease that the binding of the ligand of CCR3, such eotaxin, to the CCR3 on a target cell is an etiology.

The inventors of the present invention have zealously made studies, and have consequently discovered that a cyclic amine derivative having an arylalkyl group, a pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof, or a pharmaceutically acceptable acid addition salt thereof has an activity to inhibit the binding of the ligand of CCR3, such as the eotaxin, to a target cell, and further have found that the compounds can be used as medicines for treating or preventing diseases in which the participation of CCR3 is supposed. The studies have further been continued to accomplish the present invention.

Namely, in accordance with the present invention, there is provided a medicine, which contains, as an active ingredient, a compound represented by the following formula (I), a pharmaceutically acceptable acid addition salt thereof or a pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof, and which has a CCR³ antagonistic action,

[wherein, R¹ represents a phenyl group, a C₃ to C₈ cycloalkyl group, or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, provided that the phenyl group or the aromatic heterocyclic group in the above-mentioned R¹ may be condensed with a benzene ring, or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms to form a condensed ring, further provided that the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring may be substituted by the arbitrary number of halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, C₁ to C₆ alkyl groups, C₃ to C₈ cycloalkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, C₃ to C₅ alkylene groups, C₂ to C₄ alkylenoxy groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylthio groups, benzyl groups, benzyloxy groups, benzoylamino groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₄ to C₉ N-cycloalkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, C₃ to C₈ (alkoxycarbonyl)methyl groups, N-phenylcarbamoyl groups, piperidinocarbonyl groups, morpholinocarbonyl groups, 1-pyrrolidinylcarbonyl groups, divalent groups represented by the formula: —NH(C═O)O—, divalent groups represented by the formula: —NH(C═S)O—, amino groups, mono(C₁ to C₆ alkyl)amino groups or di(C₁ to C₆ alkyl)amino groups, and further provided that the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring may further be substituted by the arbitrary number of halogen atoms, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups.

R² represents a hydrogen atom, a C₁ to C₆ alkyl group, a C₂ to C₇ alkoxycarbonyl group, a hydroxy group or a phenyl group, provided that the C₁ to C₆ alkyl group or the phenyl group in R² may be substituted by the arbitrary number of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups, and provided that when j is 0, R² is not a hydroxy group.

j represents an integer of 0 to 2.

k represents an integer of 0 to 2.

m represents an integer of 2 to 4.

n represents 0 or 1.

R³ represents a hydrogen atom or a C₁ to C₆ alkyl group which may be substituted (by one or two phenyl groups which may be substituted by the same or different arbitrary numbers of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups, respectively).

R⁴ and R⁵, same or differently, represent a hydrogen atom, a hydroxy group, a phenyl group or a C₁ to C₆ alkyl group, respectively, and the C₁ to C₆ alkyl group in R⁴ and R⁵ may be substituted by the arbitrary number of halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, mercapto groups, guanidino groups, C₃ to C₈ cycloalkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, phenyl groups (which may be substituted by the arbitrary number of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups or benzyloxy groups), phenoxy groups, benzyloxy groups, benzyloxycarbonyl groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, amino groups, mono(C₁ to C₆ alkyl)amino groups, di(C₁ to C₆ alkyl)amino groups or aromatic heterocyclic groups (having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms) or condensed rings formed by the condensation of the aromatic heterocyclic group with a benzene ring, or R⁴ and R⁵ may together form a three to six-membered cyclic hydrocarbon.

p represents 0 or 1.

q represents 0 or 1.

G represents a group represented by —CO—, —SO₂—, —CO—O—, —NR⁷—CO—, —CO—NR⁷—, —NH—CO —NH—, —NH—CS—NH—, —NR⁷—SO₂—, —SO₂—NR⁷—, —NH—CO—O—, or —O—CO—NH—, provided that R⁷ is a hydrogen atom or a C₁ to C₆ alkyl group, or R⁷ may form a C₂ to C₅ alkylene group together with R⁵.

R⁶ represents a phenyl group, a C₃ to C₈ cycloalkyl group, a C₃ to C₆ cycloalkenyl group, a benzyl group or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, provided that the phenyl group, the benzyl group or the aromatic heterocyclic group in the above-mentioned R⁶ may be condensed, to make a condensed ring, with a benzene ring or an aromatic heterocyclic group having one or three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, further provided that the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₆ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R⁶ may be substituted by the arbitrary number of halogen atoms, hydroxy groups, mercapto groups, cyano groups, nitro groups, thiocyanato groups, carboxyl groups, carbamoyl groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₃ to C₈ cycloalkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₃ to C₈ cycloalkyloxy groups, C₁ to C₆ alkylthio groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylamino groups, benzyl groups, benzoyl groups, phenylsulfinyl groups, phenylsulfonyl groups, 3-phenylureido groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino group, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, phenylcarbamoyl groups, N,N-di(C₁ to C₆ alkyl)sulfamoyl groups, amino groups, mono(C₁ to C₆ alkyl)amino groups, di(C₁ to C₆ alkyl)amino groups, benzylamino groups, C₂ to C₇ (alkoxycarbonyl)amino groups, C₁ to C₆ (alkylsulfonyl)amino groups or bis(C₁ to C₆ alkylsulfonyl)amino groups, and further provided that the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group, or the condensed ring may further be substituted by the arbitrary number of halogen atoms, cyano groups, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, mono(C₁ to C₆ alkyl)amino groups, or di(C₁ to C₆ alkyl)amino groups.].

In accordance with the present invention, there is also provided a medicine which contains, as an active ingredient, the compound represented by the above-mentioned formula (I), the pharmaceutically acceptable acid addition salt thereof, or the pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof, and which is used for treating or preventing a disease concerned with CCR3.

The compound represented by the above-mentioned formula (I) has an activity for inhibiting that the ligand of CCR³ receptor, such as eotaxin, binds to a target cell, and an activity for inhibiting the physiological actions of the ligand of CCR3, such as the eotaxin, on the target cell. Namely, the compound represented by the above-mentioned formula (I) is a CCR3 antagonist.

BEST MODE FOR CARRYING OUT THE INVENTION

In the above-mentioned formula (I), R¹ represents a phenyl group, a C₃ to C₈ cycloalkyl group, or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, provided that the phenyl group or the aromatic heterocyclic group in the above-mentioned R¹ may be condensed with a benzene ring, or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms to form a condensed ring, further provided that the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring may be substituted by the arbitrary number of halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, C₁ to C₆ alkyl groups, C₃ to C₈ cycloalkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, C₃ to C₅ alkylene groups, C₂ to C₄ alkylenoxy groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylthio groups, benzyl groups, benzyloxy groups, benzoylamino groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₄ to C₉ N-cycloalkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, C₃ to C₈ (alkoxycarbonyl)methyl groups, N-phenylcarbamoyl groups, piperidinocarbonyl groups, morpholinocarbonyl groups, 1-pyrrolidinylcarbonyl groups, divalent groups represented by the formula: —NH(C═O)O—, divalent groups represented by the formula: —NH(C═S)O—, amino groups, mono(C₁ to C₆ alkyl)amino groups or di(C₁ to C₆ alkyl)amino groups.

“The C₃ to C₈ cycloalkyl group” in R¹ means a cyclic alkyl group such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group or a cyclooctyl group, and includes a cyclopropyl group, a cyclopentyl group, a cyclohexyl group and the like as preferable concrete examples.

“The aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms” in R¹ means an aromatic heterocyclic group such as a thienyl group, a furyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an isothiazolyl group, a pyridyl group, a pyrimidinyl group, a triazinyl group, a triazolyl group, an oxadiazolyl (furazanyl) group or a thiadiazolyl group, and includes a thienyl group, a furyl group, a pyrrolyl, an isoxazolyl group, a pyridyl group and the like as preferable concrete examples.

“The condensed ring” in R¹ means a bicyclic aromatic heterocyclic group which is formed by condensing the above-mentioned benzene ring or aromatic heterocyclic group with a benzene ring or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms at an arbitrary possible position, and includes a naphthyl group, an indolyl group, a benzofuranyl group, a benzothienyl group, a quinolyl group, a benzimidazolyl group, a benzoxazolyl group, a benzotriazolyl group, a benzoxadiazolyl (benzofurazanyl) group, a benzothiadiazolyl group and the like as preferable concrete examples.

A phenyl group, a thienyl group, a pyrazolyl group, an isoxazolyl group, a benzofuranyl group or an indolyl group is especially preferable as R¹.

“The halogen atom” as the substituent on the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring, in R¹, means a fluorine atom, a chlorine atom, a bromine atom, an iodine atom or the like.

“The C₁ to C₆ alkyl group” as the substituent of R¹ means a C₁ to C₆ straight-chain or branched alkyl group such as a methyl group, an ethyl group, a n-propyl group, a n-butyl group, a n-pentyl group, a n-hexyl group, a n-heptyl group, a n-octyl group, an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, an isohexyl group, a 2-methylpentyl group or a 1-ethylbutyl group, and includes a methyl group, an ethyl group, a propyl group, an isopropyl group and the like as preferable concrete examples.

“The C₃ to C₈ cycloalkyl group” as the substituent of R¹ is the same as the definition of “the C₃ to C₈ cycloalkyl group” in the above-mentioned R¹, and includes the same groups as preferable concrete examples.

“The C₂ to C₆ alkenyl group” as the substituent of R¹ means a C₂ to C₆ straight-chain or branched alkenyl group such as a vinyl group, an allyl group, a 1-propenyl group, a 2-butenyl group, a 3-butenyl group, a 2-methyl-1-propenyl group, a 4-pentenyl group, a 5-hexenyl group or a 4-methyl-3-pentenyl group, and includes a vinyl group, a 2-methyl-1-propenyl group and the like as preferable concrete examples.

“The C₁ to C₆ alkoxy group” as the substituent of R¹ means a group comprising the above-mentioned C₁ to C₆ alkyl group and an oxy group, and includes a methoxy group, an ethoxy group and the like as preferable concrete examples.

“The C₁ to C₆ alkylthio group” as the substituent of R¹ means a group comprising the above-mentioned C₁ to C₆ alkyl group and a thio group, and includes a methylthio group, an ethylthio group and the like as preferable concrete examples.

“The C₃ to C₅ alkylene group” as the substituent of R¹ means a C₃ to C₅ divalent alkylene group such as a trimethylene group, a tetramethylene group, a pentamethylene group or a 1-methyltrimethylene group, and includes a trimethylene group, a tetramethylene group and the like as preferable concrete examples.

“The C₂ to C₄ alkylenoxy group” as the substituent of R¹ means a group comprising a C₂ to C₄ divalent alkylene group and an oxy group, such as an ethylenoxy group (—CH₂CH₂O—), a trimethylenoxy group (—CH₂CH₂CH₂O—), a tetramethylenoxy group (—CH₂CH₂CH₂CH₂O—) or a 1,1-dimethylethylenoxy group [—CH₂C(CH₃)₂O—], and includes an ethylenoxy group, a trimethylenoxy group and the like as preferable concrete examples.

“The C₁ to C₃ alkylenedioxy group” as the substituent of R¹ means a group comprising a C₁ to C₃ divalent alkylene group and two oxy groups, such as a methylenedioxy group (—OCH₂O—), an ethylenedioxy group (—OCH₂CH₂O—), a trimethylenedioxy group (—OCH₂CH₂CH₂O—), a propylenedioxy group [—OCH₂CH(CH₃)O—], and includes a methylenedioxy group, an ethylenedioxy group and the like as preferable concrete examples.

“The C₂ to C₇ alkanoyl group” as the substituent of R¹ means a C₂ to C₇ straight-chain or branched alkanoyl group such as an acetyl group, a propanoyl group, a butanoyl group, a pentanoyl group, a hexanoyl group, a heptanoyl group, an isobutyryl group, a 3-methylbutanoyl group, a 2-methylbutanoyl group, a pivaloyl group, a 4-methylpentanoyl group, a 3,3-dimethylbutanoyl group or a 5-methylhexanoyl group, and includes an acetyl group and the like as preferable concrete examples.

“The C₂ to C₇ alkoxycarbonyl group” as the substituent of R¹ means a group comprising a C₁ to C₆ alkoxy group and a carbonyl group, and includes a methoxycarbonyl group, an ethoxycarbonyl group and the like as preferable concrete examples.

“The C₂ to C₇ alkanoyloxy group” as the substituent of R¹ means a group comprising a C₂ to C₇ alkanoyl group and an oxy group, and includes an acetyloxy group and the like as preferable concrete examples.

“The C₂ to C₇ alkanoylamino group” as the substituent of R¹ means a group comprising a C₂ to C₇ alkanoyl group and an amino group, and includes an acetylamino group and the like as preferable concrete examples.

“The C₂ to C₇ alkylcarbamoyl group” as the substituent of R¹ means a group comprising a C₁ to C₆ alkyl group and a carbamoyl group, and includes a N-methylcarbamoyl group, a N-ethylcarbamoyl group and the like as preferable concrete examples.

“The C₄ to C₉ N-cycloalkylcarbamoyl group” as the substituent of R¹ means a group comprising a C₃ to C₈ cycloalkyl group and a carbamoyl group, and includes a N-cyclopentylcarbamoyl group, a N-cyclohexylcarbamoyl group and the like as preferable concrete examples.

“The C₁ to C₆ alkylsulfonyl group” as the substituent of R¹ means a group comprising a C₁ to C₆ alkyl group and a sulfonyl group, and includes a methylsulfonyl group and the like as preferable concrete examples.

“The C₃ to C₈ (alkoxycarbonyl)methyl group” as the substituent of R¹ means a group comprising a C₂ to C₇ alkoxycarbonyl group and a methyl group, and includes a methoxycarbonylmethyl group, an ethoxycarbonylmethyl group and the like as preferable concrete examples.

“The mono(C₁ to C₆ alkyl)amino group” as the substituent of R¹ means an amino group substituted by the C₁ to C₆ alkyl group, and includes a methylamino group, an ethylamino group and the like as preferable concrete examples.

“The di(C₁ to C₆ alkyl)amino group” as the substituent of R¹ means an amino group substituted by the same or different two C₁ to C₆ alkyl groups, and includes a dimethylamino group, a diethylamino group, N-ethyl-N-methylamino group and the like as preferable concrete examples.

Among the above-mentioned groups, the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R¹ include halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, C₃ to C₅ alkylene groups, C₂ to C₄ alkylenoxy groups, methylenedioxy groups, phenyl groups, N-phenylcarbamoyl groups, amino groups and di(C₁ to C₆ alkyl)amino groups as especially preferable concrete examples. The substituents especially preferably include halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, methylenedioxy groups and N-phenylcarbamoyl groups.

Further, the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R¹ may be substituted by the arbitrary number of halogen atoms, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups. The halogen atoms, the C₁ to C₆ alkyl groups and the C₁ to C₆ alkoxy groups are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R¹, and include the same groups as preferable concrete examples.

In the formula (I), R² represents a hydrogen atom, a C₁ to C₆ alkyl group, a C₂ to C₇ alkoxycarbonyl group, a hydroxy group or a phenyl group, and the C₁ to C₆ alkyl group or the phenyl group in R² may be substituted by the arbitrary number of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups, provided that R² is not the hydroxy group, when j is 0.

The C₁ to C₆ alkyl group and the C₂ to C₇ alkoxycarbonyl group in R² are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R¹, and include the same groups as preferable concrete examples.

The halogen atoms, C₁ to C₆ alkyl groups and C₁ to C₆ alkoxy groups as the substituents of the C₁ to C₆ alkyl group or the phenyl group in R² are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R¹, and includes the same examples, respectively, as preferable concrete examples.

Among groups, a case that R² represents a hydrogen atom is most preferable.

In the formula (I), j represents an integer of 0 to 2. A case that j is 0 is most preferable.

In the formula (I), k represents an integer of 0 to 2, and m represents an integer of 2 to 4. Among them, the 2-substituted pyrrolidine compound in a case that k and m are 0 and 3, respectively, the 3-substituted pyrrolidine compound in a case that k and m are 1 and 2, respectively, the 3-substituted piperidine compound in a case that k and m are 1 and 3, respectively, 4-substituted piperidine compound in a case that k and m are 2 and 2, respectively, and the 3-substituted hexahydroazepine in a case that k and m are 1 and 4, respectively, are preferable. Especially preferably, the 3-substituted pyrrolidine compound in the case that k and m are 1 and 2, respectively, and the 4-substituted piperidine compound in the case that k and m are 2 and 2, respectively, are included.

In the formula (I), n represents 0 or 1.

Especially, the 3-amidopyrrolidine compound in a case that k, m and n are 1, 2 and 0, respectively, and the 4-(amidomethyl)piperidine in a case that k, m and n are 2, 2 and 1, respectively, are preferable.

In the formula (I), R³ represents a hydrogen atom or a C₁ to C₆ alkyl group which may be substituted (by one or two phenyl groups which may be substituted by the arbitrary number of the same or different halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups).

The C₁ to C₆ alkyl group in R³ is the same as defined as the substituent of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group, or the condensed ring in the above-mentioned R¹, and includes methyl group, ethyl group and propyl group as preferable concrete examples.

The halogen atoms, the C₁ to C₆ alkyl groups and the C₁ to C₆ alkoxy groups as the substituents of the phenyl group as the substituent of the C₁ to C₆ alkyl group in R³ are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples as preferable concrete examples.

Among them, the case in which R³ is a hydrogen atom or a non-substituted C₁ to C₆ alkyl groups,

is the most favorable.

In the formula (I), R⁴ and R⁵, same or differently, represent a hydrogen atom, a hydroxy group, a phenyl group or a C₁ to C₆ alkyl group, respectively, and the C₁ to C₆ alkyl group in R⁴ and R⁵ may be substituted by the arbitrary number of halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, mercapto groups, guanidino groups, C₃ to C₈ cycloalkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, phenyl groups (which may be substituted by the arbitrary number of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups or benzyloxy groups), phenoxy groups, benzyloxy groups, benzyloxycarbonyl groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, amino groups, mono(C₁ to C₆ alkyl)amino group, di(C₁ to C₆ alkyl)amino group, or aromatic heterocyclic groups (having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms) or condensed rings formed by condensing the aromatic heterocyclic groups with a benzene ring, or R⁴ and R⁵ may be bound to each other to form a three to six-membered cyclic hydrocarbon.

The C₁ to C₆ alkyl group in R⁴ and R⁵ is the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples as preferable concrete examples.

The halogen atom, C₁ to C₆ alkoxy group, C₁ to C₆ alkylthio group, C₂ to C₇ alkanoyl group, C₂ to C₇ alkanoyl group, C₂ to C₇ alkoxycarbonyl group, C₂ to C₇ alkanoyloxy group, C₂ to C₇ alkanoylamino group, C₂ to C₇ N-alkylcarbamoyl group, C₁ to C₆ alkylsulfonyl group, mono(C₁ to C₆ alkyl)amino group and di(C₁ to C₆ alkyl)amino group as the substituents of the C₁ to C₆ alkyl group in R⁴ and R⁵, are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples, respectively, as preferable concrete examples.

The C₃ to C₈ cycloalkyl group, and the aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen heteroatoms as the substituents of the C₁ to C₆ alkyl group in R⁴ and R⁵ are the same as defined in the above-mentioned R¹, and includes the same examples, respectively, as preferable concrete examples.

The halogen atom, the C₁ to C₆ alkyl group and the C₁ to C₆ alkoxy group as the substituents of the phenyl group as the substituent of the C₁ to C₆ alkyl group in R⁴ and R⁵, are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples, respectively, as preferable concrete examples.

The preferable concrete examples of “the three to six-membered cyclic hydrocarbon” comprising R⁴, R⁵ and the adjacent carbon atom includes cyclopropane, cyclobutane, cyclopentane and cyclohexane. Among the groups, the hydrogen atom and the C₁ to C₆ alkyl group are the especially preferable examples of R⁴ and R⁵.

In the above-mentioned formula (I), p represents 0 or 1, and q represents 0 or 1. A case that both p and q are 0 is especially preferable.

In the above-mentioned formula (I), G represents a group represented by —CO—, —SO₂—, —CO—O—, —NR⁷—CO—, —CO—NR⁷—, —NH—CO—NH—, —NH—CS—NH—, —NR⁷—SO₂—, —SO₂—NR⁷—, —NH—CO—O— or —O—CO—NH—. R⁷ represents a hydrogen atom or a C₁ to C₆ alkyl group, or R⁷ may form a C2 to C5 alkylene group together with R⁵.

The —CO—, —SO₂— and —CS— means a carbonyl group, a sulfonyl group and a thiocarbonyl group, respectively. The especially preferable example of G includes a group represented by —NR⁷—CO— and a group represented by —NH—CO—NH—.

The C₁ to C₆ alkyl group in R⁷ is the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples as preferable concrete examples.

“The C₂ to C₅ alkylene group” comprising R⁵ and R⁷ means a C₂ to C₅ straight-chain or branched alkylene group such as a methylene group, an ethylene group, a propylene group, a trimethylene group, a tetramethylene group, a 1-methyltrimethylene group or a pentamethylene group, and includes an ethylene group, a trimethylene group and a tetramethylene group as the preferable concrete examples. Among the groups, R⁷ includes the hydrogen atom as an especially preferable example.

In the above-mentioned formula (I), R⁶ represents a phenyl group, a C₃ to C₈ cycloalkyl group, a C₃ to C₆ cycloalkenyl group, a benzyl group or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, and the phenyl group, the benzyl group or the aromatic heterocyclic group in R⁶ may be condensed, to make s condensed ring, with a benzene ring or an aromatic heterocyclic group having one to three atoms of oxygen sulfur, and/or nitrogen as heteroatoms. Further, the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₆ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in R⁶ may be substituted by the arbitrary number of halogen atoms, hydroxy groups, mercapto groups, cyano groups, nitro groups, thiocyanato groups, carboxyl groups, carbamoyl groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₃ to C₈ cycloalkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₃ to C₈ cycloalkylthio groups, C₁ to C₆ alkyloxy groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylamino groups, benzyl groups, benzoyl groups, phenylsulfinyl groups, phenylsulfonyl groups, 3-phenylureido groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, phenylcarbamoyl groups, N,N-di(C₁ to C₆ alkyl)sulfamoyl groups, amino groups, mono(C₁ to C₆ alkyl)amino groups, di(C₁ to C₆ alkyl)amino groups, benzyl amino groups, C₂ to C₇ (alkoxycarbonyl)amino groups, C₁ to C₆ (alkylsulfonyl)amino groups or bis(C₁ to C₆ alkylsulfonyl)amino groups.

The C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen, and the condensed ring are the same as defined as the above-mentioned R¹, and includes the same examples, respectively, as preferable concrete examples.

“The C₃ to C₈ cycloalkenyl group” in R⁶ means a cyclic alkenyl group such as a cyclobutenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group and a cyclooctenyl group, and includes a 1-cyclopentenyl group and a 1-cyclohexenyl group as preferable concrete examples. Among the groups, R⁶ include a phenyl group, a furyl group, a thienyl group, an indolyl group and a benzofurazanyl group as especially preferable examples.

The halogen atom, the C₁ to C₆ alkyl group, the C₂ to C₆ alkenyl group, the C₁ to C₆ alkoxy group, the C₁ to C₆ alkylthio group, the C₁ to C₃ alkylenedioxy group, the C₂ to C₇ alkanoyl group, the C₂ to C₇ alkoxycarbonyl group, the C₂ to C₇ alkanoyloxy group, C₂ to C₇ alkanoylamino group, the C₂ to C₇ N-alkylcarbamoyl group, the C₁ to C₆ alkylsulfonyl group, the mono(C₁ to C₆ alkyl)amino group and the di(C₁ to C₆ alkyl)amino group as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in R⁶ are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples as preferable concrete examples.

The C₃ to C₈ cycloalkyl group as the substituent of R⁶ is the same as defined as the C₃ to C₈ cycloalkyl group in the above-mentioned R¹, and cludes the same examples as preferable concrete examples.

“The C₃ to C₈ cycloalkyloxy group” as the substituent of R⁶ means a group comprising the above-mentioned C₃ to C₈ cycloalkyl group and an oxy group, and includes a cyclopropyloxy group, a cyclopentyloxy group, a cyclohexyloxy group and the like as preferable concrete examples.

“The N,N-di(C₁ to C₆ alkyl)sulfamoyl group” as the substituent of R⁶ means a sulfamoyl group substituted by two same or different above-mentioned C₁ to C₆ alkyl groups, and includes N,N-dimethylsulfamoyl group, N,N-diethylsulfamoyl group, N-ethyl-N-methylsulfamoyl group and the like as preferable concrete examples.

“The C₂ to C₇ (alkoxycarbonyl)amino group” as the substituent of R⁶ means a group comprising the above-mentioned C₂ to C₇ alkoxycarbonyl group and an amino group, and includes a methoxycarbonylamino group, an ethoxycarbonylamino group and the like as preferable concrete examples.

“The C₁ to C₆ (alkylsulfonyl)amino group” as the substituent of R⁶ means a group comprising the above-mentioned C₁ to C₆ alkylsulfonyl group, an amino group and the like, and includes a (methylsulfonyl)amino group as a preferable concrete example.

“The bis(C₁ to C₆ alkylsulfonyl)amino group” as the substituent of R⁶ means an amino group substituted by two same or different C₁ to C₆ alkylsulfonyl groups, and includes a bis(methylsulfonyl)amino group and the like as a preferable concrete example.

Especially, the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in R⁶ include a halogen atom, a mercapto group, a nitro group, a trifluoromethyl group, a C₁ to C₆ alkyl group, a C₁ to C₆ alkoxy group, a phenyl group, a benzyloxy group, a phenylsulfinyl group, a C₂ to C₇ alkanoyl group, a C₂ to C₇ alkanoylamino group, an amino group and the like as preferable examples. The halogen atom, the nitro group, the trifluoromethyl group, the C₁ to C₆ alkyl group, the C₁ to C₆ alkoxy group, the phenylsulfinyl group and the amino group are included as especially preferable examples.

Additionally, the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in R⁶ may further be substituted by the arbitrary number of halogen atoms, cyano groups, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, mono(C₁ to C₆ alkyl)amino groups or di(C₁ to C₆ alkyl)amino groups.

The halogen atom, the C₁ to C₆ alkyl group, the C₁ to C₆ alkoxy group, the C₁ to C₆ alkylthio group, the mono(C₁ to C₆ alkyl)amino group and the di(C₁ to C₆ alkyl)amino group as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring in R⁶ are the same as defined as the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring in the above-mentioned R¹, and includes the same examples as preferable concrete examples.

By making a therapeutically effective amount of the compound represented by the above-mentioned formula (I), the pharmaceutically acceptable acid addition salt thereof or the pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof into a pharmaceutical composition together with a pharmaceutically acceptable carrier and/or a pharmaceutically acceptable diluent, the medicine for inhibiting that the ligand of CCR3, such as eotaxin, binds to the CCR3 on a target cell, the medicine for inhibiting the physiological actions of the ligand of the CCR3, such as the eotaxin, on the target cell, and further the medicine for treating or preventing diseases in which the CCR3 is supposed to participate, as the medicine of the present invention, can be prepared. Namely, the cyclic amine derivative represented by the general formula (I), the pharmaceutically acceptable acid addition thereof, or the pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof can be administered orally or parenterally such as intravenously, subcutaneously, intramuscularly, percutaneously or intrarectally.

The dosage form of the oral administration includes tablets, pills, granules, powders, liquids, suspensions and capsules.

The tablets can be prepared using a vehicle such as lactose, starch or crystalline cellulose, a binder such as carboxymethylcellulose, methylcellulose or polyvinylpyrrolidone, a disintegrator such as sodium alginate, sodium bicarbonate or sodium lauryl sulfate, and so on, by a conventional method.

The pills, the powders or the granules can also be prepared using the above-mentioned vehicle and so on by a conventional method. The liquids or the suspensions are prepared using a glycerol ester such as tricaprylin or triacetin, an alcohol such as ethanol and so on by a conventional method. The capsules are prepared by filling capsules made from gelatin or the like with the granules, the powder, the liquids or the like.

The dosage form for subcutaneous, intramuscular or intravenous administration includes injections in the forms of aqueous or non-aqueous solutions. The aqueous solutions include, for example, isotonic sodium chloride solution or the like. The non-aqueous solutions include, for example, propylene glycol, poly(ethylene glycol), olive oil, ethyl oleate or the like. The solutions, if necessary, further contain a antiseptic, a stabilizer and so on. The injections are sterilized by suitably carrying out the filtration with a bacterial filter and the treatment by the addition of a disinfectant.

The dosage form for the percutaneous administration includes an ointment and a cream. The ointment is prepared using a fatty oil or a fat such as castor oil or olive oil, petrolatum or the like by a conventional method, and the cream is prepared using a fatty oil or an emulsifier such as di(ethylene glycol) or a sorbitan monofatty acid ester by a conventional method.

Ordinary suppositories such as gelatin soft capsules are used for intrarectal administration.

The dose of the cyclic amine derivative of the present invention, the pharmaceutically acceptable acid addition salt thereof or the pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof depends on the kind of a disease, an administration route, the age and sex of the patient and the severity of a disease, but is usually 1 to 500 mg/day/adult.

The suitable concrete examples of the cyclic amine derivative of the above-mentioned formula (I) includes compounds containing substituents, respectively, shown in the following Tables 1.1 to 1.221.

In the Tables 1.1 to 1.221, “chirality” means “an absolute configuration”, namely the absolute configuration of an asymmetric carbon on the ring of the cyclic amine. “R” means that an asymmetric carbon on the ring of the cyclic amine has the absolute configuration of R, and “S” means that the asymmetric carbon has the absolute configuration of S. “-” means that the compound is a racemate or does not have an asymmetric carbon on the cyclic amine.

TABLE 1.1 Compd. No.

k m n chirality R³

1

1 2 0 — H

2

1 2 0 — H

3

1 2 0 — H

4

1 2 0 — H

5

1 2 0 S H

6

1 2 0 S H

7

1 2 0 S H

8

1 2 0 S H

9

1 2 0 S H

10

1 2 0 S H

11

1 2 0 S H

TABLE 1.2 Compd. No.

k m n chirality R³

12

1 2 0 S H

13

1 2 0 S H

14

1 2 0 S H

15

1 2 0 S H

16

1 2 0 S H

17

1 2 0 S H

18

1 2 0 S H

19

1 2 0 S H

20

1 2 0 S H

21

1 2 0 S H

22

1 2 0 S H

TABLE 1.3 Compd. No.

k m n chirality R³

23

1 2 0 S H

24

1 2 0 S H

25

1 2 0 S H

26

1 2 0 S H

27

1 2 0 S H

28

1 2 0 S H

29

1 2 0 R H

30

1 2 0 R H

31

1 2 0 R H

32

1 2 0 R H

33

1 2 0 R H

TABLE 1.4 Compd. No.

k m n chirality R³

34

1 2 0 R H

35

1 2 0 R H

36

1 2 0 R H

37

1 2 0 R H

38

1 2 0 R H

39

1 2 0 R H

40

1 2 0 R H

41

1 2 0 R H

42

1 2 0 R H

43

1 2 0 R H

44

1 2 0 R H

TABLE 1.5 Compd. No.

k m n chirality R³

45

1 2 0 R H

46

1 2 0 R H

47

1 2 0 R H

48

1 2 0 R H

49

1 2 0 R H

50

1 2 0 R H

51

1 2 0 R H

52

1 2 0 R H

53

1 2 0 R H

54

1 2 0 R H

55

1 2 0 R H

TABLE 1.6 Compd. No.

k m n chirality R³

56

1 2 0 R H

57

1 2 0 R H

58

1 2 0 R H

59

1 2 0 R H

60

1 2 0 R H

61

1 2 0 R H

62

1 2 0 R H

63

1 2 0 R H

64

1 2 0 R H

65

1 2 0 R H

66

1 2 0 R H

TABLE 1.7 Compd. No.

k m n chirality R³

67

1 2 0 R H

68

1 2 0 R H

69

1 2 0 R H

70

1 2 0 R H

71

1 2 0 R H

72

1 2 0 R H

73

1 2 0 R H

74

1 2 0 R H

75

1 2 0 R H

76

1 2 0 R H

77

1 2 0 R H

TABLE 1.8 Compd. No.

k m n chirality R³

78

1 2 0 R H

79

1 2 0 R H

80

1 2 0 R H

81

1 2 0 R H

82

1 2 0 — —CH₃

83

1 2 0 R H

84

1 2 0 R H

85

1 2 0 — H

86

1 2 0 — H

87

1 2 0 S H

88

1 2 0 S H

TABLE 1.9 Compd. No.

k m n chirality R³

89

1 2 0 S H

90

1 2 0 S H

91

1 2 0 S H

92

1 2 0 S H

93

1 2 0 S H

94

1 2 0 S H

95

1 2 0 S H

96

1 2 0 S H

97

1 2 0 S H

98

1 2 0 S H

99

1 2 0 S H

TABLE 1.10 Compd. No.

k m n chirality R³

100

1 2 0 S H

101

1 2 0 S H

102

1 2 0 S H

103

1 2 0 S H

104

1 2 0 S H

105

1 2 0 S H

106

1 2 0 S H

107

1 2 0 S H

108

1 2 0 S H

109

1 2 0 S H

110

1 2 0 S H

TABLE 1.11 Compd. No.

k m n chirality R³

111

1 2 0 R H

112

1 2 0 R H

113

1 2 0 R H

114

1 2 0 R H

115

1 2 0 R H

116

1 2 0 R H

117

1 2 0 R H

118

1 2 0 R H

119

1 2 0 R H

120

1 2 0 R H

121

1 2 0 R H

TABLE 1.12 Compd. No.

k m n chirality R³

122

1 2 0 R H

123

1 2 0 R H

124

1 2 0 R H

125

1 2 0 R H

126

1 2 0 R H

127

1 2 0 R H

128

1 2 0 R H

129

1 2 0 R H

130

1 2 0 R H

131

1 2 0 R H

132

1 2 0 R H

TABLE 1.13 Compd. No.

k m n chirality R³

133

1 2 0 R H

134

1 2 0 R H

135

1 2 0 R H

136

1 2 0 R H

137

1 2 0 R H

138

1 2 0 R H

139

1 2 0 R H

140

1 2 0 R H

141

1 2 0 R H

142

1 2 0 R H

143

1 2 0 R H

TABLE 1.14 Compd. No.

k m n chirality R³

144

1 2 0 R H

145

1 2 0 R H

146

1 2 0 R H

147

1 2 0 R H

148

1 2 0 R H

149

1 2 0 R H

150

1 2 0 R H

151

1 2 0 R H

152

1 2 0 R H

153

1 2 0 R H

154

1 2 0 R H

TABLE 1.15 Compd. No.

k m n chirality R³

155

1 2 0 R H

156

1 2 0 R H

157

1 2 0 R H

158

1 2 0 R H

159

1 2 0 R H

160

1 2 0 R H

161

1 2 0 R H

162

1 2 0 R H

163

1 2 0 R H

164

1 2 0 R H

165

1 2 0 R H

TABLE 1.16 Compd. No.

k m n chirality R³

166

1 2 0 R H

167

1 2 0 R H

168

1 2 0 R H

169

1 2 0 R H

170

1 2 0 R H

171

1 2 0 R H

172

1 2 0 R H

173

1 2 0 R H

174

1 2 0 R H

175

1 2 0 R H

176

1 2 0 R H

TABLE 1.17 Compd. No.

k m n chirality R³

177

1 2 0 R H

178

1 2 0 R H

179

1 2 0 R H

180

1 2 0 R H

181

1 2 0 R H

182

1 2 0 R H

183

1 2 0 R H

184

1 2 0 R H

185

1 2 0 R H

186

1 2 0 R H

187

1 2 0 R H

TABLE 1.18 Compd. No.

k m n chirality R³

188

1 2 0 R H

189

1 2 0 R H

190

1 2 0 R H

191

1 2 0 R H

192

1 2 0 R H

193

1 2 0 R H

194

1 2 0 R H

195

1 2 0 R H

196

1 2 0 R H

197

1 2 0 R H

198

1 2 0 R H

TABLE 1.19 Compd. No.

k m n chirality R³

199

1 2 0 R H

200

1 2 0 R H

201

1 2 0 R H

202

1 2 0 R H

203

1 2 0 R H

204

1 2 0 R H

205

1 2 0 R H

206

1 2 0 R H

207

1 2 0 R H

208

1 2 0 R H

209

1 2 0 R H

TABLE 1.20 Compd. No.

k m n chirality R³

210

1 2 0 R H

211

1 2 0 R H

212

1 2 0 R H

213

1 2 0 R H

214

1 2 0 - H

215

1 2 0 - H

216

1 2 0 - H

217

1 2 0 - H

218

1 2 0 - H

219

1 2 0 - H

220

1 2 0 - H

TABLE 1.21 Compd. No.

k m n chirality R³

221

1 2 0 - H

222

1 2 0 - H

223

1 2 0 - H

224

1 2 0 - H

225

1 2 0 - H

226

1 2 0 - H

227

1 2 0 - H

228

1 2 0 - H

229

1 2 0 - H

230

1 2 0 - H

231

1 2 0 - H

TABLE 1.22 Compd. No.

k m n chirality R³

232

1 2 0 - H

233

1 2 0 - H

234

1 2 0 - H

235

1 2 0 - H

236

1 2 0 - H

237

1 2 0 - H

238

1 2 0 - H

239

1 2 0 S H

240

1 2 0 S H

241

1 2 0 S H

242

1 2 0 S H

TABLE 1.23 Compd. No.

k m n chirality R³

243

1 2 0 S H

244

1 2 0 S H

245

1 2 0 S H

246

1 2 0 S H

247

1 2 0 S H

248

1 2 0 S H

249

1 2 0 S H

250

1 2 0 S H

251

1 2 0 S H

252

1 2 0 S H

253

1 2 0 S H

TABLE 1.24 Compd. No.

k m n chirality R³

254

1 2 0 S H

255

1 2 0 S H

256

1 2 0 S H

257

1 2 0 S H

258

1 2 0 S H

259

1 2 0 S H

260

1 2 0 S H

261

1 2 0 S H

262

1 2 0 S H

263

1 2 0 S H

264

1 2 0 S H

TABLE 1.25 Compd. No.

k m n chirality R³

265

1 2 0 S H

266

1 2 0 S H

267

1 2 0 S H

268

1 2 0 S H

269

1 2 0 S H

270

1 2 0 S H

271

1 2 0 S H

272

1 2 0 S H

273

1 2 0 S H

274

1 2 0 S H

275

1 2 0 S H

TABLE 1.26 Compd. No.

k m n chirality R³

276

1 2 0 S H

277

1 2 0 S H

278

1 2 0 S H

279

1 2 0 S H

280

1 2 0 S H

281

1 2 0 S H

282

1 2 0 S H

283

1 2 0 S H

284

1 2 0 S H

285

1 2 0 R H

286

1 2 0 R H

TABLE 1.27 Compd. No.

k m n chirality R³

287

1 2 0 R H

288

1 2 0 R H

289

1 2 0 R H

290

1 2 0 R H

291

1 2 0 R H

292

1 2 0 R H

293

1 2 0 R H

294

1 2 0 R H

295

1 2 0 R H

296

1 2 0 R H

297

1 2 0 R H

TABLE 1.28 Compd. No.

k m n chirality R³

298

1 2 0 R H

299

1 2 0 R H

300

1 2 0 R H

301

1 2 0 R H

302

1 2 0 R H

303

1 2 0 R H

304

1 2 0 R H

305

1 2 0 R H

306

1 2 0 R H

307

1 2 0 R H

308

1 2 0 R H

TABLE 1.29 Compd. No.

k m n chirality R³

309

1 2 0 R H

310

1 2 0 R H

311

1 2 0 R H

312

1 2 0 R H

313

1 2 0 R H

314

1 2 0 R H

315

1 2 0 R H

316

1 2 0 R H

317

1 2 0 R H

318

1 2 0 R H

319

1 2 0 R H

TABLE 1.30 Compd. No.

k m n chirality R³

320

1 2 0 R H

321

1 2 0 R H

322

1 2 0 R H

323

1 2 0 R H

324

1 2 0 R H

325

1 2 0 R H

326

1 2 0 R H

327

1 2 0 R H

328

1 2 0 R H

329

1 2 0 R H

330

0 3 1 — H

TABLE 1.31 Compd. No.

k m n chirality R³

331

0 3 1 — H

332

0 3 1 — H

333

0 3 1 — H

334

0 3 1 — H

335

0 3 1 — H

336

0 3 1 — H

337

0 3 1 — H

338

0 3 1 — H

339

0 3 1 R H

340

0 3 1 S H

341

0 3 1 — H

TABLE 1.32 Compd. No.

k m n chirality R³

342

0 3 1 — H

343

0 3 1 — H

344

0 3 1 — H

345

0 3 1 — H

346

0 3 1 — H

347

0 3 1 — H

348

0 3 1 — H

349

0 3 1 — H

350

0 3 1 — H

351

0 3 1 — H

352

0 3 1 — H

TABLE 1.33 Compd. No.

k m n chirality R³

353

1 2 1 — H

354

1 3 0 — H

355

1 3 0 — H

356

1 3 0 — H

357

1 3 0 — H

358

1 3 0 — H

359

1 3 0 — H

360

1 3 0 — H

361

1 3 0 — H

362

1 3 0 — H

363

1 3 0 — H

TABLE 1.34 Compd. No.

k m n chirality R³

364

1 3 0 — H

365

1 3 0 — H

366

1 3 0 — H

367

1 3 0 — H

368

1 3 0 — H

369

1 3 0 — H

370

1 3 0 — H

371

1 3 0 — H

372

1 3 0 — H

373

1 3 0 — H

374

1 3 0 — H

TABLE 1.35 Compd. No.

k m n chirality R³

375

1 3 0 — H

376

1 3 0 — H

377

1 3 0 — H

378

1 3 0 — H

379

1 3 0 — H

380

1 3 0 — H

381

1 3 0 — H

382

1 3 0 — H

383

1 3 0 — H

384

2 2 0 — H

385

2 2 0 — H

TABLE 1.36 Compd. No.

k m n chirality R³

386

2 2 0 — H

387

2 2 0 — H

388

2 2 0 — H

389

2 2 0 — H

390

2 2 0 — H

391

2 2 0 — H

392

2 2 0 — H

393

2 2 0 — H

394

2 2 0 — H

395

2 2 0 — H

396

2 2 0 — H

TABLE 1.37 Compd. No.

k m n chirality R³

397

2 2 0 — H

398

2 2 0 — H

399

2 2 0 — H

400

2 2 0 — H

401

2 2 0 — H

402

2 2 0 — H

403

2 2 0 — H

404

2 2 0 — H

405

2 2 0 — H

406

2 2 0 — H

407

2 2 0 — H

TABLE 1.38 Compd. No.

k m n chirality R³

408

2 2 0 — H

409

2 2 0 — H

410

2 2 0 — H

411

2 2 0 — H

412

2 2 0 — H

413

2 2 0 — H

414

2 2 0 — H

415

2 2 0 — H

416

2 2 0 — H

417

2 2 0 — H

418

2 2 0 — H

TABLE 1.39 Compd. No.

k m n chirality R³

419

2 2 0 — H

420

2 2 0 — H

421

2 2 0 — H

422

2 2 0 — H

423

2 2 0 — H

424

2 2 0 — H

425

2 2 0 — H

426

2 2 0 — H

427

2 2 0 — H

428

2 2 0 — H

429

2 2 0 — H

TABLE 1.40 Compd. No.

k m n chirality R³

430

2 2 0 — H

431

2 2 0 — H

432

2 2 0 — H

433

2 2 0 — H

434

1 3 1 — H

435

1 3 1 — H

436

1 3 1 — H

437

1 3 1 — H

438

1 3 1 — H

439

1 3 1 — H

440

1 3 1 — H

TABLE 1.41 Compd. No.

k m n chirality R³

441

1 3 1 — H

442

1 3 1 — H

443

1 3 1 — H

444

1 3 1 — H

445

1 3 1 — H

446

1 3 1 — H

447

1 3 1 — H

448

1 3 1 — H

449

1 3 1 — H

450

1 3 1 — H

451

1 3 1 — H

TABLE 1.42 Compd. No.

k m n chirality R³

452

1 3 1 — H

453

1 3 1 — H

454

1 3 1 — H

455

1 3 1 — H

456

1 3 1 — H

457

1 3 1 — H

458

2 2 1 — H

459

2 2 1 — H

460

2 2 1 — H

461

2 2 1 — H

462

2 2 1 — H

TABLE 1.43 Compd. No.

k m n chirality R³

463

2 2 1 — H

464

2 2 1 — H

465

2 2 1 — H

466

2 2 1 — H

467

2 2 1 — H

468

2 2 1 — H

469

2 2 1 — H

470

2 2 1 — H

471

2 2 1 — H

472

2 2 1 — H

473

2 2 1 — H

TABLE 1.44 Compd. No.

k m n chirality R³

474

2 2 1 — H

475

2 2 1 — H

476

2 2 1 — H

477

2 2 1 — H

478

2 2 1 — H

479

2 2 1 — H

480

2 2 1 — H

481

2 2 1 — H

482

2 2 1 — H

483

2 2 1 — H

484

2 2 1 — H

TABLE 1.45 Compd. No.

k m n chirality R³

485

2 2 1 — H

486

2 2 1 — H

487

2 2 1 — H

488

2 2 1 — H

489

2 2 1 — H

490

2 2 1 — H

491

2 2 1 — H

492

2 2 1 — H

493

2 2 1 — H

494

2 2 1 — H

495

2 2 1 — H

TABLE 1.46 Compd. No.

k m n chirality R³

496

2 2 1 — H

497

2 2 1 — H

498

2 2 1 — H

499

2 2 1 — H

500

2 2 1 — H

501

2 2 1 — H

502

2 2 1 — H

503

2 2 1 — H

504

2 2 1 — H

505

2 2 1 — H

506

2 2 1 — H

TABLE 1.47 Compd. No.

k m n chirality R³

507

2 2 1 — H

508

2 2 1 — H

509

2 2 1 — H

510

2 2 1 — H

511

2 2 1 — H

512

2 2 1 — H

513

2 2 1 — H

514

2 2 1 — H

515

2 2 1 — H

516

2 2 1 — H

517

2 2 1 — H

TABLE 1.48       Compd. No.

        k         m         n         chirality 518

2 2 1 — 519

2 2 1 — 520

2 2 1 — 521

2 2 1 — 522

2 2 1 — 523

2 2 1 — 524

2 2 1 — 525

2 2 1 — 526

2 2 1 — 527

2 2 1 — 528

2 2 1 —       Compd. No.         R³

518 H

519 H

520 —CH₃

521

522

523

524

525 H

526 H

527 H

528 H

TABLE 1.49 Compd. No.

k m n chirality R³

529

2 2 1 — H

530

2 2 1 — H

531

2 2 1 — H

532

2 2 1 — H

533

2 2 1 — H

534

2 2 1 — H

535

2 2 1 — H

536

2 2 1 — H

537

2 2 1 — H

538

2 2 1 — H

539

2 2 1 — H

TABLE 1.50 Compd. No.

k m n chirality R³

540

2 2 1 — H

541

2 2 1 — H

542

2 2 1 — H

543

2 2 1 — H

544

2 2 1 — H

545

2 2 1 — H

546

2 2 1 — H

547

2 2 1 — H

548

2 2 1 — H

549

2 2 1 — H

550

2 2 1 — H

TABLE 1.51 Compd. No.

k m n chirality R³

551

2 2 1 — H

552

2 2 1 — H

553

2 2 1 — H

554

2 2 1 — H

555

2 2 1 — H

556

2 2 1 — H

557

2 2 1 — H

558

2 2 1 — H

559

2 2 1 — H

560

2 2 1 — H

561

2 2 1 — H

TABLE 1.52 Compd. No.

k m n chirality R³

562

2 2 1 — H

563

2 2 1 — H

564

2 2 1 — H

565

2 2 1 — H

566

2 2 1 — H

567

2 2 1 — H

566

2 2 1 — H

569

2 2 1 — H

570

2 2 1 — H

571

2 2 1 — H

572

2 2 1 — H

TABLE 1.53 Compd. No.

k m n chirality R³

573

2 2 1 — H

574

2 2 1 — H

575

2 2 1 — H

576

2 2 1 — H

577

2 2 1 — H

578

2 2 1 — H

579

2 2 1 — H

580

2 2 1 — H

581

2 2 1 — H

582

2 2 1 — H

583

2 2 1 — H

TABLE 1.54 Compd. No.

k m n chirality R³

584

2 2 1 — H

585

2 2 1 — H

586

2 2 1 — H

587

2 2 1 — H

588

2 2 1 — H

589

2 2 1 — H

590

2 2 1 — H

591

2 2 1 — H

592

2 2 1 — H

593

2 2 1 — H

594

2 2 1 — H

TABLE 1.55 Compd. No.

k m n chirality R³

595

2 2 1 — H

596

2 2 1 — H

597

2 2 1 — H

598

2 2 1 — H

599

2 2 1 — H

600

2 2 1 — H

601

2 2 1 — H

602

2 2 1 — H

603

2 2 1 — H

604

2 2 1 — H

605

2 2 1 — H

TABLE 1.56 Compd. No.

k m n chirality R³

606

2 2 1 — H

607

2 2 1 — H

608

2 2 1 — H

609

2 2 1 — H

610

2 2 1 — H

611

2 2 1 — H

612

2 2 1 — H

613

2 2 1 — H

614

2 2 1 — H

615

2 2 1 — H

616

2 2 1 — H

TABLE 1.57 Compd. No.

k m n chirality R³

617

2 2 1 — H

618

2 2 1 — H

619

2 2 1 — H

620

2 2 1 — H

621

2 2 1 — H

622

2 2 1 — H

623

2 2 1 — H

624

2 2 1 — H

625

2 2 1 — H

626

2 2 1 — H

627

2 2 1 — H

TABLE 1.58 Compd. No.

k m n chirality R³

628

2 2 1 — H

629

2 2 1 — H

630

2 2 1 — H

631

2 2 1 — H

632

2 2 1 — H

633

2 2 1 — H

634

2 2 1 — H

635

2 2 1 — H

636

2 2 1 — H

637

2 2 1 — H

638

2 2 1 — H

TABLE 1.59 Compd. No.

k m n chirality R³

639

2 2 1 — H

640

2 2 1 — H

641

2 2 1 — H

642

2 2 1 — H

643

2 2 1 — H

644

2 2 1 — H

645

2 2 1 — H

646

2 2 1 — H

647

2 2 1 — H

648

2 2 1 — H

649

2 2 1 — H

TABLE 1.60 Compd. No.

k m n chirality R³

650

2 2 1 — H

651

2 2 1 — H

652

2 2 1 — H

653

2 2 1 — H

654

2 2 1 — H

655

2 2 1 — H

656

2 2 1 — H

657

2 2 1 — H

658

2 2 1 — H

659

2 2 1 — H

660

2 2 1 — H

TABLE 1.61 Compd. No.

k m n chirality R³

661

2 2 1 — H

662

2 2 1 — H

663

2 2 1 — H

664

2 2 1 — H

665

2 2 1 — H

666

2 2 1 — H

667

2 2 1 — H

668

2 2 1 — H

669

2 2 1 — H

670

2 2 1 — H

671

2 2 1 — H

TABLE 1.62 Compd. No.

k m n chirality R³

672

2 2 1 — H

673

2 2 1 — H

674

2 2 1 — H

675

2 2 1 — H

676

2 2 1 — H

677

2 2 1 — H

678

2 2 1 — H

679

2 2 1 — H

680

2 2 1 — H

681

2 2 1 — H

682

2 2 1 — H

TABLE 1.63 Compd. No.

k m n chirality R³

683

2 2 1 — H

684

2 2 1 — H

685

2 2 1 — H

686

2 2 1 — H

687

2 2 1 — H

688

2 2 1 — H

689

2 2 1 — H

690

2 2 1 — H

691

2 2 1 — H

692

2 2 1 — H

693

2 2 1 — H

TABLE 1.64 Compd. No.

k m n chirality R³

694

2 2 1 — H

695

2 2 1 — H

696

2 2 1 — H

697

2 2 1 — H

698

2 2 1 — H

699

2 2 1 — H

700

2 2 1 — H

701

2 2 1 — H

702

2 2 1 — H

703

2 2 1 — H

704

2 2 1 — H

TABLE 1.65 Compd. No.

k m n chirality R³

705

2 2 1 — H

706

2 2 1 — H

707

2 2 1 — H

708

2 2 1 — H

709

2 2 1 — H

710

2 2 1 — H

711

2 2 1 — H

712

2 2 1 — H

713

2 2 1 — H

714

2 2 1 — H

715

2 2 1 — H

TABLE 1.66 Compd. No.

k m n chirality R³

716

2 2 1 — H

717

2 2 1 — H

718

2 2 1 — H

719

2 2 1 — H

720

2 2 1 — H

721

2 2 1 — H

722

2 2 1 — H

723

2 2 1 — H

724

2 2 1 — H

725

2 2 1 — H

726

2 2 1 — H

TABLE 1.67 Compd. No.

k m n chirality R³

727

2 2 1 — H

728

2 2 1 — H

729

2 2 1 — H

730

2 2 1 — H

731

2 2 1 — H

732

2 2 1 — H

733

2 2 1 — H

734

2 2 1 — H

735

2 2 1 — H

736

2 2 1 — H

737

2 2 1 — H

TABLE 1.68 Compd. No.

k m n chirality R³

738

2 2 1 — H

739

2 2 1 — H

740

2 2 1 — H

741

2 2 1 — H

742

2 2 1 — H

743

2 2 1 — H

744

2 2 1 — H

745

2 2 1 — H

746

2 2 1 — H

747

2 2 1 — H

748

2 2 1 — H

TABLE 1.69 Compd. No.

k m n chirality R³

749

2 2 1 — H

750

2 2 1 — H

751

2 2 1 — H

752

2 2 1 — H

753

2 2 1 — H

754

2 2 1 — H

755

2 2 1 — H

756

2 2 1 — H

757

2 2 1 — H

758

2 2 1 — H

759

2 2 1 — H

TABLE 1.70 Compd. No.

k m n chirality R³

760

2 2 1 — H

761

2 2 1 — H

762

2 2 1 — H

763

2 2 1 — H

764

2 2 1 — H

765

2 2 1 — H

766

2 2 1 — H

767

2 2 1 — H

768

2 2 1 — H

769

2 2 1 — H

770

2 2 1 — H

TABLE 1.71 Compd. No.

k m n chirality R³

771

2 2 1 — H

772

2 2 1 — H

773

2 2 1 — H

774

2 2 1 — H

775

2 2 1 — H

776

2 2 1 — H

777

2 2 1 — H

778

2 2 1 — H

779

2 2 1 — H

780

2 2 1 — H

781

2 2 1 — H

TABLE 1.72 Compd. No.

k m n chirality R³

782

2 2 1 — H

783

2 2 1 — H

784

2 2 1 — H

785

2 2 1 — H

786

2 2 1 — H

787

2 2 1 — H

788

2 2 1 — H

789

2 2 1 — H

790

2 2 1 — H

791

2 2 1 — H

792

2 2 1 — H

TABLE 1.73 Compd. No.

k m n chirality R³

793

2 2 1 — H

794

2 2 1 — H

795

2 2 1 — H

796

2 2 1 — H

797

2 2 1 — H

798

2 2 1 — H

799

2 2 1 — H

800

2 2 1 — H

801

2 2 1 — H

802

2 2 1 — H

803

2 2 1 — H

TABLE 1.74 Compd. No.

k m n chirality R³

804

2 2 1 — H

805

2 2 1 — H

806

2 2 1 — H

807

2 2 1 — H

808

2 2 1 — H

809

2 2 1 — H

810

2 2 1 — H

811

2 2 1 — H

812

2 2 1 — H

813

2 2 1 — H

814

2 2 1 — H

TABLE 1.75 Compd. No.

k m n chirality R³

815

2 2 1 — H

816

2 2 1 — H

817

2 2 1 — H

818

2 2 1 — H

819

2 2 1 — H

820

2 2 1 — H

821

2 2 1 — H

822

2 2 1 — H

823

2 2 1 — H

824

2 2 1 — H

825

2 2 1 — H

TABLE 1.76 Compd. No.

k m n chirality R³

826

2 2 1 — H

827

2 2 1 — H

828

2 2 1 — H

829

2 2 1 — H

830

2 2 1 — H

831

2 2 1 — H

832

2 2 1 — H

833

2 2 1 — H

834

2 2 1 — H

835

2 2 1 — H

836

2 2 1 — H

TABLE 1.77 Compd. No.

k m n chirality R³

837

2 2 1 — H

838

2 2 1 — H

839

2 2 1 — H

840

2 2 1 — H

841

2 2 1 — H

842

2 2 1 — H

843

2 2 1 — H

844

2 2 1 — H

845

2 2 1 — H

846

2 2 1 — H

847

2 2 1 — H

TABLE 1.78 Compd. No.

k m n chirality R³

848

2 2 1 — H

849

2 2 1 — H

850

2 2 1 — H

851

2 2 1 — H

852

2 2 1 — H

853

2 2 1 — H

854

2 2 1 — H

855

2 2 1 — H

856

2 2 1 — H

857

2 2 1 — H

858

2 2 1 — H

TABLE 1.79 Compd. No.

k m n chirality R³

859

2 2 1 — H

860

2 2 1 — H

861

2 2 1 — H

862

2 2 1 — H

863

2 2 1 — H

864

2 2 1 — H

865

2 2 1 — H

866

2 2 1 — H

867

2 2 1 — H

868

2 2 1 — H

869

2 2 1 — H

TABLE 1.80 Compd. No.

k m n chirality R³

870

2 2 1 — H

871

2 2 1 — H

872

2 2 1 — H

873

2 2 1 — H

874

2 2 1 — H

875

2 2 1 — H

876

2 2 1 — H

877

2 2 1 — H

878

2 2 1 — H

879

2 2 1 — H

880

2 2 1 — H

TABLE 1.81 Compd. No.

k m n chirality R³

881

2 2 1 — H

882

2 2 1 — H

883

2 2 1 — H

884

2 2 1 — H

885

2 2 1 — H

886

2 2 1 — H

887

2 2 1 — H

888

2 2 1 — H

889

2 2 1 — H

890

2 2 1 — H

891

2 2 1 — H

TABLE 1.82 Compd. No.

k m n chirality R³

892

2 2 1 — H

893

2 2 1 — H

894

2 2 1 — H

895

2 2 1 — H

896

2 2 1 — H

897

2 2 1 — H

898

2 2 1 — H

899

2 2 1 — H

900

2 2 1 — H

901

2 2 1 — H

902

2 2 1 — H

TABLE 1.83 Compd. No.

k m n chirality R³

903

2 2 1 — H

904

2 2 1 — H

905

2 2 1 — H

906

2 2 1 — H

907

2 2 1 — H

908

2 2 1 — H

909

2 2 1 — H

910

2 2 1 — H

911

2 2 1 — H

912

2 2 1 — H

913

2 2 1 — H

TABLE 1.84 Compd. No.

k m n chirality R³

914

2 2 1 — H

915

2 2 1 — H

916

2 2 1 — H

917

2 2 1 — H

918

2 2 1 — H

919

2 2 1 — H

920

2 2 1 — H

921

2 2 1 — H

922

2 2 1 — H

923

2 2 1 — H

924

2 2 1 — H

TABLE 1.85 Compd. No.

k m n chirality R³

925

2 2 1 — H

926

2 2 1 — H

927

2 2 1 — H

928

2 2 1 — H

929

2 2 1 — H

930

2 2 1 — H

931

2 2 1 — H

932

2 2 1 — H

933

2 2 1 — H

934

2 2 1 — H

935

2 2 1 — H

TABLE 1.86 Compd. No.

k m n chirality R³

936

2 2 1 — H

937

2 2 1 — H

938

2 2 1 — H

939

2 2 1 — H

940

2 2 1 — H

941

2 2 1 — H

942

2 2 1 — H

943

1 4 0 — H

944

1 4 0 — H

945

1 4 0 — H

946

1 4 0 — H

TABLE 1.87 Compd. No.

k m n chirality R³

947

1 4 0 — H

948

1 4 0 — H

949

1 4 0 — H

950

0 4 1 — H

951

1 2 0 R H

952

1 2 0 R H

953

1 2 0 R H

954

1 2 0 R H

955

1 2 0 R H

956

1 2 0 R H

957

1 2 0 R H

TABLE 1.88 Compd. No.

k m n chirality R³

958

1 2 0 R H

959

1 2 0 R H

960

1 2 0 R H

961

1 2 0 R H

962

1 2 0 R H

963

1 2 0 R H

964

1 2 0 R H

965

1 4 0 R H

966

1 4 0 R H

967

1 4 0 R H

968

1 4 0 R H

TABLE 1.89 Compd. No.

k m n chirality R³

969

1 2 0 R H

970

1 2 0 R H

971

1 2 0 R H

972

1 2 0 R H

973

1 2 0 R H

974

1 2 0 R H

975

1 2 0 R H

976

1 4 0 R H

977

1 4 0 R H

978

1 4 0 R H

979

1 4 0 R H

TABLE 1.90 Compd. No.

k m n chirality R³

980

1 2 0 R H

981

1 2 0 R H

982

1 2 0 R H

983

1 2 0 R H

984

1 2 0 R H

985

1 2 0 R H

986

1 2 0 R H

987

2 2 1 — H

988

1 4 0 — H

989

1 4 0 — H

990

1 4 0 — H

TABLE 1.91 Compd. No.

k m n chirality R³

 991

1 4 0 — H

 992

1 4 0 — H

 993

1 4 0 — H

 994

1 4 0 — H

 995

1 4 0 — H

 996

1 4 0 — H

 997

2 2 1 — H

 998

2 2 1 — H

 999

2 2 1 — H

1000

2 2 1 — H

1001

2 2 1 — H

TABLE 1.92 Compd. No.

k m n chirality R³

1002

2 2 1 — H

1003

2 2 1 — H

1004

2 2 1 — H

1005

2 2 1 — H

1006

2 2 1 — H

1007

2 2 1 — H

1008

2 2 1 — H

1009

2 2 1 — H

1010

2 2 1 — H

1011

2 2 1 — H

1012

2 2 1 — H

TABLE 1.93 Compd. No.

k m n chirality R³

1013

2 2 1 — H

1014

2 2 1 — H

1015

2 2 1 — H

1016

2 2 0 — H

1017

2 2 0 — H

1018

2 2 1 — H

1019

2 2 1 — H

1020

2 2 1 — H

1021

2 2 1 — H

1022

2 2 1 — H

1023

2 2 1 — H

TABLE 1.94 Compd. No.

k m n chirality R³

1024

2 2 1 — H

1025

2 2 1 — H

1026

2 2 1 — H

1027

2 2 1 — H

1028

2 2 1 — H

1029

2 2 1 — H

1030

2 2 1 — H

1031

2 2 1 — H

1032

2 2 1 — H

1033

2 2 1 — H

1034

2 2 1 — H

TABLE 1.95 Compd. No.

k m n chirality R³

1035

2 2 1 — H

1036

2 2 1 — H

1037

2 2 1 — H

1038

2 2 1 — H

1039

2 2 1 — H

1040

2 2 1 — H

1041

2 2 1 — H

1042

2 2 1 — H

1043

2 2 1 — H

1044

2 2 1 — H

1045

2 2 1 — H

TABLE 1.96 Compd. No.

k m n chirality R³

1046

2 2 1 — H

1047

2 2 1 — H

1048

2 2 1 — H

1049

2 2 1 — H

1050

2 2 1 — H

1051

2 2 1 — H

1052

2 2 1 — H

1053

2 2 1 — H

1054

2 2 1 — H

1055

2 2 1 — H

1056

2 2 1 — H

TABLE 1.97 Compd. No.

k m n chirality R³

1057

2 2 1 — H

1058

2 2 1 — H

1059

2 2 1 — H

1060

2 2 1 — H

1061

2 2 1 — H

1062

2 2 1 — H

1063

2 2 1 — H

1064

2 2 1 — H

1065

2 2 1 — H

1066

2 2 1 — H

1067

2 2 1 — H

TABLE 1.98 Compd. No.

k m n chirality R³

1068

2 2 1 — H

1069

2 2 1 — H

1070

2 2 1 — H

1071

2 2 1 — H

1072

2 2 1 — H

1073

2 2 1 — H

1074

2 2 1 — H

1075

2 2 1 — H

1076

2 2 1 — H

1077

2 2 1 — H

1078

2 2 1 — H

TABLE 1.99 Compd. No.

k m n chirality R³

1079

2 2 1 — H

1080

2 2 1 — H

1081

2 2 1 — H

1082

2 2 1 — H

1083

2 2 1 — H

1084

1 2 0 R H

1085

1 2 0 R H

1086

1 2 0 R H

1087

1 2 0 R H

1088

1 2 0 R H

1089

1 2 0 R H

TABLE 1.100 Compd. No.

k m n chirality R³

1090

2 2 1 — H

1091

2 2 1 — H

1092

2 2 1 — H

1093

2 2 0 — H

1094

2 2 0 — H

1095

2 2 1 — H

1096

2 2 1 — H

1097

2 2 1 — H

1098

2 2 1 — H

1099

2 2 1 — H

1100

2 2 1 — H

TABLE 1.101 Compd. No.

k m n chirality R³

1101

1 2 0 R H

1102

1 2 0 R H

1103

1 2 0 R H

1104

1 2 0 R H

1105

1 2 0 R H

1106

1 2 0 R H

1107

1 2 0 R H

1108

1 2 0 R H

1109

1 2 0 R H

1110

1 2 0 R H

1111

1 2 0 R H

TABLE 1.102 Compd. No.

k m n chirality R³

1112

1 2 0 R H

1113

2 2 1 — H

1114

2 2 1 — H

1115

2 2 1 — H

1116

2 2 1 — H

1117

2 2 1 — H

1118

1 2 0 R H

1119

1 2 0 R H

1120

1 2 0 R H

1121

1 2 0 R H

1122

1 2 0 R H

TABLE 1.103 Compd. No.

k m n chirality R³

1123

1 2 0 R H

1124

1 2 0 R H

1125

2 2 1 — H

1126

2 2 1 — H

1127

2 2 1 — H

1128

2 2 1 — H

1129

2 2 1 — H

1130

2 2 1 — H

1131

2 2 1 — H

1132

2 2 1 — H

1133

1 2 0 R H

TABLE 1.104 Compd. No.

k m n chirality R³

1134

1 2 0 R H

1135

1 2 0 R H

1136

1 2 0 R H

1137

1 2 0 R H

1138

1 2 0 R H

1139

1 2 0 R H

1140

1 2 0 R H

1141

1 2 0 R H

1142

1 2 0 R H

1143

1 2 0 R H

1144

1 2 0 R H

TABLE 1.105 Compd. No.

k m n chirality R³

1145

1 2 0 R H

1146

1 2 0 R H

1147

1 2 0 R H

1148

1 2 0 R H

1149

1 2 0 R H

1150

1 2 0 R H

1151

1 2 0 R H

1152

1 2 0 R H

1153

1 2 0 R H

1154

1 2 0 R H

1155

1 2 0 R H

TABLE 1.106 Compd. No.

k m n chirality R³

1156

1 2 0 R H

1157

1 2 0 R H

1158

1 2 0 R H

1159

1 2 0 R H

1160

1 2 0 R H

1161

1 2 0 R H

1162

1 2 0 R H

1163

1 2 0 R H

1164

1 2 0 R H

1165

1 2 0 R H

1166

1 2 0 R H

TABLE 1.107 Compd. No.

k m n chirality R³

1167

2 2 1 — H

1168

1 2 0 R H

1169

1 2 0 R H

1170

1 2 0 R H

1171

1 2 0 R H

1172

1 2 0 R H

1173

1 2 0 R H

1174

1 2 0 R H

1175

1 2 0 R H

1176

1 2 0 R H

1177

1 2 0 R H

TABLE 1.108 Compd. No.

k m n chirality R³

1178

1 2 0 R H

1179

1 2 0 R H

1180

1 2 0 R H

1181

1 2 0 R H

1182

1 2 0 R H

1183

1 2 0 R H

1184

1 2 0 R H

1185

1 2 0 R H

1186

1 2 0 R H

1187

2 2 1 — H

1188

2 2 1 — H

TABLE 1.109 Compd. No.

k m n chirality R³

1189

2 2 1 — H

1190

2 2 1 — H

1191

1 2 0 R H

1192

1 2 0 R H

1193

1 2 0 R H

1194

1 2 0 R H

1195

1 2 0 R H

1196

1 2 0 R H

1197

1 2 0 R H

1198

1 2 0 R H

1199

1 2 0 R H

TABLE 1.110 Compd. No.

k m n chirality R³

1200

1 2 0 R H

1201

1 2 0 R H

1202

1 2 0 R H

1203

1 2 0 R H

1204

1 2 0 R H

1205

1 2 0 R H

1206

1 2 0 R H

1207

1 2 0 R H

1208

1 2 0 R H

1209

1 2 0 R H

1210

1 2 0 R H

TABLE 1.111 Compd. No.

k m n chirality R³

1211

1 2 0 R H

1212

1 2 0 R H

1213

2 2 1 — H

1214

2 2 1 — H

1215

2 2 1 — H

1216

2 2 1 — H

1217

1 2 0 R H

1218

1 2 0 R H

1219

1 2 0 R H

1220

1 2 0 R H

1221

1 2 0 R H

TABLE 1.112 Compd. No.

k m n chirality R³

1222

1 2 0 R H

1223

1 2 0 R H

1224

1 2 0 R H

1225

1 2 0 R H

1226

1 2 0 R H

1227

1 2 0 R H

1228

1 2 0 R H

1229

1 2 0 R H

1230

1 2 0 R H

1231

1 2 0 R H

1232

1 2 0 R H

TABLE 1.113 Compd. No.

k m n chirality R³

1233

1 2 0 R H

1234

1 2 0 R H

1235

1 2 0 R H

1236

1 2 0 R H

1237

1 2 0 R H

1238

1 2 0 R H

1239

1 2 0 R H

1240

1 2 0 R H

1241

2 2 1 — H

1242

2 2 1 — H

1243

2 2 1 — H

TABLE 1.114 Compd. No.

k m n chirality R³

1244

2 2 1 — H

1245

2 2 1 — H

1246

2 2 1 — H

1247

2 2 1 — H

1248

2 2 1 — H

1249

1 2 0 R H

1250

1 2 0 R H

1251

1 2 0 R H

1252

1 2 0 R H

1253

1 2 0 R H

1254

1 2 0 R H

TABLE 1.115 Compd. No.

k m n chirality R³

1255

1 2 0 R H

1256

1 2 0 R H

1257

1 2 0 R H

1258

1 2 0 R H

1259

1 2 0 R H

1260

1 2 0 R H

1261

1 2 0 R H

1262

1 2 0 R H

1263

1 2 0 R H

1264

1 2 0 R H

1265

1 2 0 R H

TABLE 1.116 Compd. No.

k m n chirality R³

1266

1 2 0 R H

1267

1 2 0 R H

1268

1 2 0 R H

1269

1 2 0 R H

1270

1 2 0 R H

1271

1 2 0 R H

1272

1 2 0 R H

1273

1 2 0 R H

1274

1 2 0 R H

1275

1 2 0 R H

1276

1 2 0 R H

TABLE 1.117 Compd. No.

k m n chirality R³

1277

1 2 0 R H

1278

1 2 0 R H

1279

1 2 0 R H

1280

1 2 0 R H

1281

1 2 0 R H

1282

2 2 1 — H

1283

2 2 1 — H

1284

2 2 1 — H

1285

2 2 1 — H

1286

1 2 0 R H

1287

1 2 0 R H

TABLE 1.118 Compd. No.

k m n chirality R³

1288

1 2 0 R H

1289

1 2 0 R H

1290

1 2 0 R H

1291

1 2 0 R H

1292

1 2 0 R H

1293

1 2 0 R H

1294

1 2 0 R H

1295

1 2 0 R H

1296

1 2 0 R H

1297

1 2 0 R H

1298

1 2 0 R H

TABLE 1.119 Compd. No.

k m n chirality R³

1299

1 2 0 R H

1300

1 2 0 R H

1301

1 2 0 R H

1302

1 2 0 R H

1303

1 2 0 R H

1304

1 2 0 R H

1305

1 2 0 R H

1306

1 2 0 R H

1307

1 2 0 R H

1308

1 2 0 R H

1309

1 2 0 R H

TABLE 1.120 Compd. No.

k m n chirality R³

1310

1 2 0 R H

1311

1 2 0 R H

1312

1 2 0 R H

1313

1 2 0 R H

1314

1 2 0 R H

1315

1 2 0 R H

1316

1 2 0 R H

1317

1 2 0 R H

1318

1 2 0 R H

1319

1 2 0 R H

1320

1 2 0 R H

TABLE 1.121 Compd. No.

k m n chirality R³

1321

1 2 0 R H

1322

1 2 0 R H

1323

1 2 0 R H

1324

1 2 0 R H

1325

1 2 0 R H

1326

1 2 0 R H

1327

1 2 0 R H

1328

1 2 0 R H

1329

1 2 0 R H

1330

1 2 0 R H

1331

1 2 0 R H

TABLE 1.122 Compd. No.

k m n chirality R³

1332

1 2 0 R H

1333

1 2 0 R H

1334

1 2 0 R H

1335

1 2 0 R H

1336

1 2 0 R H

1337

1 2 0 R H

1338

1 2 0 R H

1339

1 2 0 R H

1340

1 2 0 R H

1341

1 2 0 R H

1342

2 2 1 — H

TABLE 1.123 Compd. No.

k m n chirality R³

1343

2 2 1 — H

1344

2 2 1 — H

1345

2 2 1 — H

1346

2 2 1 — H

1347

1 2 0 R H

1348

1 2 0 R H

1349

1 2 0 R H

1350

2 2 1 — H

1351

1 2 0 R H

1352

1 2 0 R H

1353

1 2 0 R H

TABLE 1.124 Compd. No.

k m n chirality R³

1354

2 2 1 — H

1355

1 2 0 R H

1356

1 2 0 R H

1357

1 2 0 R H

1358

2 2 1 — H

1359

1 2 0 R H

1360

1 2 0 R H

1361

1 2 0 R H

1362

1 2 0 R H

1363

1 2 0 R H

1364

1 2 0 R H

TABLE 1.125 Compd. No.

k m n chirality R³

1365

1 2 0 R H

1366

1 2 0 R H

1367

1 2 0 R H

1368

1 2 0 R H

1369

1 2 0 R H

1370

1 2 0 R H

1371

1 2 0 R H

1372

1 2 0 R H

1373

1 2 0 R H

1374

1 2 0 R H

1375

1 2 0 R H

TABLE 1.126 Compd. No.

k m n chirality R³

1376

1 2 0 R H

1377

1 2 0 R H

1378

1 2 0 R H

1379

1 2 0 R H

1380

1 2 0 R H

1381

1 2 0 R H

1382

1 2 0 R H

1383

2 2 1 — H

1384

2 2 1 — H

1385

2 2 1 — H

1386

2 2 1 — H

TABLE 1.127 Compd. No.

k m n chirality R³

1387

1 2 0 R H

1388

1 2 0 R H

1389

1 2 0 R H

1390

1 2 0 R H

1391

1 2 0 R H

1392

1 2 0 R H

1393

1 2 0 R H

1394

1 2 0 R H

1395

1 2 0 R H

1396

1 2 0 R H

1397

1 2 0 R H

TABLE 1.128 Compd. No.

k m n chirality R³

1398

1 2 0 R H

1399

1 2 0 R H

1400

1 2 0 R H

1401

1 2 0 R H

1402

1 2 0 R H

1403

1 2 0 R H

1404

1 2 0 R H

1405

1 2 0 R H

1406

1 2 0 R H

1407

1 2 0 R H

1408

1 2 0 R H

TABLE 1.129 Compd. No.

k m n chirality R³

1409

1 2 0 R H

1410

1 2 0 R H

1411

1 2 0 R H

1412

1 2 0 R H

1413

1 2 0 R H

1414

2 2 1 — H

1415

1 2 0 R H

1416

1 2 0 R H

1417

1 2 0 R H

1418

2 2 1 — H

1419

1 2 0 R H

TABLE 1.130 Compd. No.

k m n chirality R³

1420

1 2 0 R H

1421

1 2 0 R H

1422

2 2 1 — H

1423

1 2 0 R H

1424

1 2 0 R H

1425

1 2 0 R H

1426

2 2 1 — H

1427

2 2 1 — H

1428

2 2 1 — H

1429

2 2 1 — H

1430

2 2 1 — H

TABLE 1.131 Compd. No.

k m n chirality R³

1431

2 2 1 — H

1432

2 2 1 — H

1433

2 2 1 — H

1434

2 2 1 — H

1435

2 2 1 — H

1436

2 2 1 — H

1437

2 2 1 — H

1438

2 2 1 — H

1439

2 2 1 — H

1440

2 2 1 — H

1441

2 2 1 — H

TABLE 1.132 Compd. No.

k m n chirality R³

1442

2 2 1 — H

1443

2 2 1 — H

1444

2 2 1 — H

1445

2 2 1 — H

1446

2 2 1 — H

1447

2 2 1 — H

1448

2 2 1 — H

1449

2 2 1 — H

1450

2 2 1 — H

1451

2 2 1 — H

1452

2 2 1 — H

TABLE 1.133 Compd. No.

k m n chirality R³

1453

2 2 1 — H

1454

2 2 1 — H

1455

2 2 1 — H

1456

2 2 1 — H

1457

2 2 1 — H

1458

2 2 1 — H

1459

2 2 1 — H

1460

2 2 1 — H

1461

2 2 1 — H

1462

2 2 1 — H

1463

2 1 1 — H

TABLE 1.134 Compd. No.

k m n chirality R³

1464

2 1 1 — H

1465

2 1 1 — H

1466

2 1 1 — H

1467

2 1 1 — H

1468

2 1 1 — H

1469

2 1 1 — H

1470

2 1 1 — H

1471

2 1 1 — H

1472

1 2 0 R H

1473

1 2 0 R H

1474

1 2 0 R H

TABLE 1.135 Compd. No.

k m n chirality R³

1475

1 2 0 R H

1476

1 2 0 R H

1477

1 2 0 R H

1478

1 2 0 R H

1479

1 2 0 R H

1480

1 2 0 R H

1481

1 2 0 R H

1482

1 2 0 R H

1483

1 2 0 R H

1484

1 2 0 R H

1485

1 2 0 R H

TABLE 1.136 Compd. No.

k m n chirality R³

1486

1 2 0 R H

1487

1 2 0 R H

1488

1 2 0 R H

1489

1 2 0 R H

1490

1 2 0 R H

1491

1 2 0 R H

1492

1 2 0 R H

1493

1 2 0 R H

1494

1 2 0 R H

1495

1 2 0 R H

1496

1 2 0 R H

TABLE 1.137 Compd. No.

k m n chirality R³

1497

1 2 0 R H

1498

1 2 0 R H

1499

1 2 0 R H

1500

1 2 0 R H

1501

1 2 0 R H

1502

1 2 0 R H

1503

1 2 0 R H

1504

1 2 0 R H

1505

1 2 0 R H

1506

2 1 1 — H

1507

2 1 1 — H

TABLE 1.138 Compd. No.

k m n chirality R³

1508

2 1 1 — H

1509

2 1 1 — H

1510

2 1 1 — H

1511

2 1 1 — H

1512

2 1 1 — H

1513

2 1 1 — H

1514

2 2 1 — H

1515

2 2 1 — H

1516

2 2 1 — H

1517

2 2 1 — H

1518

2 2 1 — H

TABLE 1.139 Compd. No.

k m n chirality R³

1519

2 2 1 — H

1520

1 2 0 R H

1521

1 2 0 R H

1522

1 2 0 R H

1523

1 2 0 R H

1524

1 2 0 R H

1525

1 2 0 R H

1526

1 2 0 R H

1527

1 2 0 R H

1528

1 2 0 R H

1529

1 2 0 R H

TABLE 1.140 Compd. No.

k m n chirality R³

1530

1 2 0 R H

1531

1 2 0 R H

1532

1 2 0 R H

1533

1 2 0 R H

1534

1 2 0 R H

1535

1 2 0 R H

1536

1 2 0 R H

1537

1 2 0 R H

1538

1 2 0 R H

1539

1 2 0 R H

1540

1 2 0 R H

TABLE 1.141 Compd. No.

k m n chirality R³

1541

1 2 0 R H

1542

1 2 0 R H

1543

1 2 0 R H

1544

1 2 0 R H

1545

1 2 0 R H

1546

1 2 0 R H

1547

1 2 0 R H

1548

1 2 0 R H

1549

1 2 0 R H

1550

1 2 0 R H

1551

1 2 0 R H

TABLE 1.142 Compd. No.

k m n chirality R³

1552

1 2 0 R H

1553

1 2 0 R H

1554

1 2 0 R H

1555

1 2 0 R H

1556

1 2 0 R H

1557

1 2 0 R H

1558

1 2 0 R H

1559

1 2 0 R H

1560

1 2 0 R H

1561

1 2 0 R H

1562

1 2 0 R H

TABLE 1.143       Compd. No.

        k         m         n 1563

1 2 0 1564

1 2 0 1565

1 2 0 1566

1 2 0 1567

1 2 0 1568

1 2 0 1569

1 2 0 1570

2 2 1 1571

2 2 1 1572

2 2 1 1573

2 2 1       Compd. No.         chirality         R³

1563 R H

1564 R H

1565 R H

1566 R H

1567 R H

1568 R H

1569 R H

1570 — H

1571 — H

1572 — H

1573 — H

TABLE 1.144 Compd. No.

k m n chirality R³

1574

2 2 1 — H

1575

2 2 1 — H

1576

2 2 1 — H

1577

2 2 1 — H

1578

2 2 1 — H

1579

2 2 1 — H

1580

2 2 1 — H

1581

2 2 1 — H

1582

2 2 1 — H

1583

1 2 0 R H

1584

1 2 0 R H

TABLE 1.145 Compd. No.

k m n chirality R³

1585

1 2 0 R H

1586

1 2 0 R H

1587

1 2 0 R H

1588

1 2 0 R H

1589

1 2 0 R H

1590

1 2 0 R H

1591

1 2 0 R H

1592

1 2 0 R H

1593

1 2 0 R H

1594

1 2 0 R H

1595

1 2 0 R H

TABLE 1.146 Compd. No.

k m n chirality R³

1596

1 2 0 R H

1597

1 2 0 R H

1598

1 2 0 R H

1599

1 2 0 R H

1600

2 2 1 — H

1601

2 2 1 — H

1602

2 2 1 — H

1603

2 2 1 — H

1604

2 2 1 — H

1605

2 2 1 — H

1606

1 2 0 R H

TABLE 1.147 Compd. No.

k m n chirality R³

1607

1 2 0 R H

1608

1 2 0 R H

1609

2 2 1 — H

1610

2 2 1 — H

1611

2 2 1 — H

1612

2 2 1 — H

1613

2 2 1 — H

1614

1 2 0 R H

1615

2 2 1 — H

1616

2 2 1 — H

1617

2 2 1 — H

TABLE 1.148 Compd. No.

k m n chirality R³

1618

1 2 0 R H

1619

1 2 0 R H

1620

1 2 0 R H

1621

1 2 0 R H

1622

1 2 0 R H

1623

1 2 0 R H

1624

1 2 0 R H

1625

1 2 0 R H

1626

1 2 0 R H

1627

1 2 0 R H

1628

1 2 0 R H

TABLE 1.149 Compd. No.

k m n chirality R³

1629

1 2 0 R H

1630

1 2 0 R H

1631

1 2 0 R H

1632

1 2 0 R H

1633

1 2 0 R H

1634

1 2 0 R H

1635

1 2 0 R H

1636

1 2 0 R H

1637

1 2 0 R H

1638

1 2 0 R H

1639

1 2 0 R H

TABLE 1.150 Compd. No.

k m n chirality R³

1640

1 2 0 R H

1641

1 2 0 R H

1642

1 2 0 R H

1643

1 2 0 R H

1644

1 2 0 R H

1645

1 2 0 R H

1646

1 2 0 R H

1647

2 2 1 — H

1648

1 2 0 R H

1649

2 2 1 — H

1650

1 2 0 R H

TABLE 1.151 Compd. No.

k m n chirality R³

1651

2 2 1 — H

1652

2 2 1 — H

1653

2 2 1 — H

1654

2 2 1 — H

1655

2 2 1 — H

1656

2 2 1 — H

1657

2 2 1 — H

1658

2 2 1 — H

1659

2 2 1 — H

1660

1 2 0 R H

1661

1 2 0 R H

TABLE 1.152 Compd. No.

k m n chirality R³

1662

1 2 0 R H

1663

1 2 0 R H

1664

2 2 1 — H

1665

2 2 1 — H

1666

2 2 1 — H

1667

2 2 1 — H

1668

2 2 1 — H

1669

2 2 1 — H

1670

2 2 1 — H

1671

2 2 1 — H

1672

2 2 1 — H

TABLE 1.153 Compd. No.

k m n chirality R³

1673

2 2 1 — H

1674

2 2 1 — H

1675

2 2 1 — H

1676

2 2 1 — H

1677

2 2 1 — H

1678

2 2 1 — H

1679

2 2 1 — H

1680

2 2 1 — H

1681

2 2 1 — H

1682

2 2 1 — H

1683

2 2 1 — H

TABLE 1.154 Compd. No.

k m n chirality R³

1684

2 2 1 — H

1685

2 2 1 — H

1686

2 2 1 — H

1687

2 2 1 — H

1688

2 2 1 — H

1689

2 2 1 — H

1690

2 2 1 — H

1691

2 2 1 — H

1692

1 2 0 R H

1693

1 2 0 R H

1694

1 2 0 R H

TABLE 1.155 Compd. No.

k m n chirality R³

1695

1 2 0 R H

1696

1 2 0 R H

1697

1 2 0 R H

1698

1 2 0 R H

1699

1 2 0 R H

1700

1 2 0 R H

1701

1 2 0 R H

1702

1 2 0 R H

1703

1 2 0 R H

1704

1 2 0 R H

1705

1 2 0 R H

TABLE 1.156 Compd. No.

k m n chirality R³

1706

1 2 0 R H

1707

1 2 0 R H

1708

1 2 0 R H

1709

1 2 0 R H

1710

1 2 0 R H

1711

1 2 0 R H

1712

1 2 0 R H

1713

1 2 0 R H

1714

1 2 0 R H

1715

1 2 0 R H

1716

1 2 0 R H

TABLE 1.157 Compd. No.

k m n chirality R³

1717

1 2 0 R H

1718

1 2 0 R H

1719

1 2 0 R H

1720

1 2 0 R H

1721

1 2 0 R H

1722

1 2 0 R H

1723

1 2 0 R H

1724

1 2 0 R H

1725

1 2 0 R H

1726

1 2 0 R H

1727

1 2 0 R H

TABLE 1.158 Compd. No.

k m n chirality R³

1728

1 2 0 R H

1729

1 2 0 R H

1730

1 2 0 R H

1731

1 2 0 R H

1732

1 2 0 R H

1733

1 2 0 R H

1734

1 2 0 R H

1735

1 2 0 R H

1736

1 2 0 R H

1737

1 2 0 R H

1738

1 2 0 R H

TABLE 1.159 Compd. No.

k m n chirality R³

1739

1 2 0 R H

1740

1 2 0 R H

1741

1 2 0 R H

1742

1 2 0 R H

1743

1 2 0 R H

1744

1 2 0 R H

1745

1 2 0 R H

1746

1 2 0 R H

1747

1 2 0 R H

1748

1 2 0 R H

1749

1 2 0 R H

TABLE 1.160 Compd. No.

k m n chirality R³

1750

1 2 0 R H

1751

1 2 0 R H

1752

1 2 0 R H

1753

1 2 0 R H

1754

1 2 0 R H

1755

1 2 0 R H

1756

1 2 0 R H

1757

1 2 0 R H

1758

1 2 0 R H

1759

1 2 0 R H

1760

1 2 0 R H

TABLE 1.161 Compd. No.

k m n chirality R³

1761

1 2 0 R H

1762

1 2 0 R H

1763

2 2 0 — H

1764

2 2 0 — H

1765

2 2 0 — H

1766

2 2 0 — H

1767

1 3 1 — H

1768

1 3 1 — H

1769

1 2 0 R H

1770

1 2 0 R H

1771

1 2 0 R H

TABLE 1.162 Compd. No.

k m n chirality 1772

1 2 0 R 1773

1 2 0 R 1774

1 2 0 R 1775

1 2 0 R 1776

1 2 0 R 1777

2 2 1 — 1778

2 2 1 — 1779

2 2 1 — 1780

2 2 1 — 1781

2 2 1 — 1782

2 2 1 — Compd. No. R³

1772 H

1773 H

1774 H

1775 H

1776 H

1777 H

1778 H

1779 H

1780 H

1781 H

1782 H

TABLE 1.163 Compd. No.

k m n chirality R³

1783

2 2 1 — H

1784

2 2 1 — H

1785

2 2 1 — H

1786

2 2 1 — H

1787

1 2 0 R H

1788

2 2 1 — H

1789

2 2 1 — H

1790

1 2 0 S H

1791

1 2 0 S H

1792

2 2 1 — H

1793

2 2 1 — H

TABLE 1.164 Compd. No.

k m n chirality R³

1794

2 2 1 — H

1795

2 2 1 — H

1798

2 2 1 — H

1797

2 2 1 — H

1798

2 2 1 — H

1799

2 2 1 — H

1800

2 2 1 — H

1801

2 2 1 — H

1802

1 2 0 R H

1803

1 2 0 R H

1804

2 2 1 — H

TABLE 1.165 Compd. No.

k m n chirality R³

1805

1 2 0 R H

1806

1 2 0 R H

1807

1 2 0 R H

1808

1 2 0 R H

1809

1 2 0 R H

1810

1 2 0 R H

1811

1 2 0 R H

1812

1 2 0 R H

1813

1 2 0 R H

1814

1 2 0 R H

1815

1 2 0 R H

TABLE 1.166 Compd. No.

k m n chirality R³

1816

1 2 0 R H

1817

1 2 0 R H

1818

1 2 0 R H

1819

1 2 0 R H

1820

1 2 0 R H

1821

1 2 0 R H

1822

1 2 0 R H

1823

1 2 0 R H

1824

1 2 0 R H

1825

1 2 0 R H

1826

1 2 0 R H

TABLE 1.167 Compd. No.

k m n chirality R³

1327

1 2 0 R H

1328

1 2 0 R H

1829

1 2 0 R H

1330

1 2 0 R H

1831

1 2 0 R H

1832

1 2 0 R H

1833

1 2 0 R H

1834

1 2 0 R H

1835

1 2 0 R H

1836

1 2 0 R H

1837

1 2 0 R H

TABLE 1.168 Compd. No.

k m n chirality R³

1838

1 2 0 R H

1839

1 2 0 R H

1840

1 2 0 R H

1841

1 2 0 R H

1842

1 2 0 R H

1843

1 2 0 R H

1844

1 2 0 R H

1845

1 2 0 R H

1846

1 2 0 R H

1847

1 2 0 R H

1848

1 2 0 R H

TABLE 1.169 Compd. No.

k m n chirality R³

1849

1 2 0 R H

1850

1 2 0 R H

1851

1 2 0 R H

1852

1 2 0 R H

1853

1 2 0 R H

1854

1 2 0 R H

1855

1 2 0 R H

1856

1 2 0 R H

1857

1 2 0 R H

1858

1 2 0 R H

1859

1 2 0 R H

TABLE 1.170 Compd. No.

k m n chirality R³

1860

1 2 0 R H

1861

1 2 0 R H

1662

1 2 0 R H

1863

1 2 0 R H

1864

1 2 0 R H

1865

1 2 0 R H

1866

1 2 0 R H

1867

1 2 0 R H

1868

1 2 0 R H

1869

1 2 0 R H

1870

1 2 0 R H

TABLE 1.171 Compd. No.

k m n chirality R³

1871

1 2 0 R H

1872

1 2 0 R H

1873

1 2 0 R H

1874

1 2 0 R H

1875

1 2 0 R H

1876

1 2 0 R H

1877

1 2 0 R H

1878

1 2 0 R H

1879

1 2 0 R H

1880

1 2 0 R H

1881

1 2 0 R H

TABLE 1.172 Compd. No.

k m n chirality R³

1882

1 2 0 R H

1883

1 2 0 R H

1884

1 2 0 R H

1885

1 2 0 R H

1886

1 2 0 R H

1887

1 2 0 R H

1888

1 2 0 R H

1889

1 2 0 R H

1890

1 2 0 R H

1891

1 2 0 R H

1892

1 2 0 R H

TABLE 1.173 Compd. No.

k m n chirality R³

1893

1 2 0 R H

1894

1 2 0 R H

1895

1 2 0 R H

1896

1 2 0 R H

1897

1 2 0 R H

1898

1 2 0 R H

1899

1 2 0 R H

1900

1 2 0 R H

1901

1 2 0 R H

1902

1 2 0 R H

1903

2 2 1 — H

TABLE 1.174 Compd. No.

k m n chirality R³

1904

2 2 1 — H

1905

1 2 0 R H

1906

1 2 0 R H

1907

1 2 0 R H

1908

1 2 0 R H

1909

1 2 0 R H

1910

2 2 1 — H

1911

2 2 1 — H

1912

2 2 1 — H

1913

2 2 1 — H

1914

2 2 1 — H

TABLE 1.175 Compd. No.

k m n chirality R³

1915

1 2 0 R H

1916

1 2 0 R H

1917

2 2 1 — H

1918

2 2 1 — H

1919

2 2 1 — H

1920

2 2 1 — H

1921

1 2 0 R H

1922

2 2 1 — H

1923

2 2 1 — H

1924

2 2 1 — H

1925

2 2 1 — H

TABLE 1.176 Compd. No.

k m n chirality R³

1926

2 2 1 — H

1927

2 2 1 — H

1928

2 2 1 — H

1929

2 2 1 — H

1930

2 2 1 — H

1931

2 2 1 — H

1932

2 2 1 — H

1933

2 2 1 — H

1934

2 2 1 — H

1935

2 2 1 — H

1936

2 2 1 — H

TABLE 1.177 Compd. No.

k m n chirality R³

1937

2 2 1 — H

1938

2 2 1 — H

1939

2 2 1 — H

1940

2 2 1 — H

1941

2 2 1 — H

1942

2 2 1 — H

1943

2 2 1 — H

1944

2 2 1 — H

1945

2 2 1 — H

1946

2 2 1 — H

1947

2 2 1 — H

TABLE 1.178 Compd. No.

k m n chirality R³

1948

2 2 1 — H

1949

2 2 1 — H

1950

2 2 1 — H

1951

2 2 1 — H

1952

2 2 1 — H

1953

2 2 1 — H

1954

2 2 1 — H

1955

2 2 1 — H

1956

2 2 1 — H

1957

2 2 1 — H

1958

2 2 1 — H

TABLE 1.179 Compd. No.

k m n chirality R³

1959

2 2 1 — H

1960

2 2 1 — H

1961

2 2 1 — H

1962

2 2 1 — H

1963

2 2 1 — H

1964

2 2 1 — H

1965

2 2 1 — H

1966

2 2 1 — H

1967

2 2 1 — H

1968

2 2 1 — H

1969

2 2 1 — H

TABLE 1.180 Compd. No.

k m n chirality R³

1970

2 2 1 — H

1971

2 2 1 — H

1972

2 2 1 — H

1973

2 2 1 — H

1974

2 2 1 — H

1975

2 2 1 — H

1976

2 2 1 — H

1977

2 2 1 — H

1978

2 2 1 — H

1979

2 2 1 — H

1980

2 2 1 — H

TABLE 1.181 Compd. No.

k m n chirality R³

1981

2 2 1 — H

1982

2 2 1 — H

1983

2 2 1 — H

1984

2 2 1 — H

1985

2 2 1 — H

1986

2 2 1 — H

1987

2 2 1 — H

1988

2 2 1 — H

1989

2 2 1 — H

1990

2 2 1 — H

1991

2 2 1 — H

TABLE 1.182 Compd. No.

k m n chirality R³

1992

2 2 1 — H

1993

2 2 1 — H

1994

2 2 1 — H

1995

2 2 1 — H

1996

2 2 1 — H

1997

2 2 1 — H

1998

2 2 1 — H

1999

2 2 1 — H

2000

2 2 1 — H

2001

2 2 1 — H

2002

2 2 1 — H

TABLE 1.183 Compd. No.

k m n chirality R³

2003

2 2 1 — H

2004

2 2 1 — H

2005

2 2 1 — H

2006

2 2 1 — H

2007

2 2 1 — H

2008

2 2 1 — H

2009

2 2 1 — H

2010

2 2 1 — H

2011

2 2 1 — H

2012

2 2 1 — H

2013

2 2 1 — H

TABLE 1.184 Compd. No.

k m n chirality R³

2014

2 2 1 — H

2015

2 2 1 — H

2016

2 2 1 — H

2017

2 2 1 — H

2018

2 2 1 — H

2019

2 2 1 — H

2020

2 2 1 — H

2021

2 2 1 — H

2022

2 2 1 — H

2023

2 2 1 — H

2024

2 2 1 — H

TABLE 1.185 Compd. No.

k m n chirality R³

2025

2 2 1 — H

2026

2 2 1 — H

2027

2 2 1 — H

2028

2 2 1 — H

2029

2 2 1 — H

2030

2 2 1 — H

2031

2 2 1 — H

2032

2 2 1 — H

2033

2 2 1 — H

2034

2 2 1 — H

2035

2 2 1 — H

TABLE 1.186 Compd. No.

k m n chirality R³

2036

2 2 1 — H

2037

2 2 1 — H

2033

2 2 1 — H

2039

2 2 1 — H

2040

1 2 0 R H

2041

1 2 0 R H

2042

1 2 0 R H

2043

1 2 0 R H

2044

1 2 0 R H

2045

1 2 0 R H

2046

1 2 0 R H

TABLE 1.187 Compd. No.

k m n chirality R³

2047

1 2 0 R H

2048

1 2 0 R H

2049

1 2 0 R H

2050

1 2 0 R H

2051

1 2 0 R H

2052

2 2 1 — H

2053

2 2 1 — H

2054

2 2 1 — H

2055

2 2 1 — H

2056

2 2 1 — H

2057

2 2 1 — H

TABLE 1.188 Compd. No.

k m n chirality R³

2058

2 2 1 — H

2059

2 2 1 — H

2060

2 2 1 — H

2061

2 2 1 — H

2062

2 2 1 — H

2063

2 2 1 — H

2064

2 2 1 — H

2065

2 2 1 — H

2066

2 2 1 — H

2067

2 2 1 — H

2068

2 2 1 — H

TABLE 1.189 Compd. No.

k m n chirality R³

2069

2 2 1 — H

2070

2 2 1 — H

2071

2 2 1 — H

2072

2 2 1 — H

2073

2 2 1 — H

2074

2 2 1 — H

2075

2 2 1 — H

2076

2 2 1 — H

2077

2 2 1 — H

2078

2 2 1 — H

2079

2 2 1 — H

TABLE 1.190 Compd. No.

k m n chirality R³

2080

2 2 1 — H

2081

2 2 1 — H

2082

2 2 1 — H

2083

1 2 0 R H

2084

1 2 0 R H

2085

1 2 0 R H

2086

1 2 0 R H

2087

1 2 0 R H

2088

1 2 0 R H

2089

1 2 0 R H

2090

1 2 0 R H

TABLE 1.191 Compd. No.

k m n chirality R³

2091

2 2 1 — H

2092

2 2 1 — H

2093

2 2 1 — H

2094

2 2 1 — H

2095

2 2 1 — H

2096

2 2 1 — H

2097

2 2 1 — H

2098

2 2 1 — H

2099

2 2 1 — H

2100

2 2 1 — H

2101

2 2 1 — H

TABLE 1.192 Compd. No.

k m n chirality R³

2102

2 2 1 — H

2103

2 2 1 — H

2104

2 2 1 — H

2105

2 2 1 — H

2106

2 2 1 — H

2107

2 2 1 — H

2108

2 2 1 — H

2109

2 2 1 — H

2110

2 2 1 — H

2111

2 2 1 — H

2112

2 2 1 — H

TABLE 1.193 Compd. No.

k m n chirality R³

2113

2 2 1 — H

2114

2 2 1 — H

2115

2 2 1 — H

2116

2 2 1 — H

2117

2 2 1 — H

2118

1 2 0 R H

2119

1 2 0 R H

2120

1 2 0 R H

2121

1 2 0 R H

2122

1 2 0 R H

2123

1 2 0 R H

TABLE 1.194 Compd. No.

k m n chirality R³

2124

1 2 0 R H

2125

1 2 0 R H

2126

1 2 0 R H

2127

1 2 0 R H

2128

1 2 0 R H

2129

1 2 0 R H

2130

2 2 1 — H

2131

2 2 1 — H

2132

1 2 0 R H

2133

1 2 0 R H

2134

1 2 0 R H

TABLE 1.195 Compd. No.

k m n chirality R³

2135

1 2 0 R H

2136

1 2 0 R H

2137

1 2 0 R H

2138

1 2 0 R H

2139

1 2 0 R H

2140

2 2 1 — H

2141

2 2 1 — H

2142

2 2 1 — H

2143

2 2 1 — H

2144

2 2 1 — H

2145

2 2 1 — H

TABLE 1.196 Compd. No.

k m n chirality R³

2146

2 2 1 — H

2147

2 2 1 — H

2148

2 2 1 — H

2149

1 2 0 R H

2150

1 2 0 R H

2151

1 2 0 R H

2152

1 2 0 R H

2153

1 2 0 R H

2154

2 2 1 — H

2155

2 2 1 — H

2156

2 2 1 — H

TABLE 1.197 Compd. No.

k m n chirality R³

2157

1 2 0 R H

2158

1 2 0 R H

2159

2 2 1 — H

2160

2 2 1 — H

2161

2 2 1 — H

2162

2 2 1 — H

2163

2 2 1 — H

2164

1 2 0 R H

2165

1 2 0 R H

2166

1 2 0 R H

2167

1 2 0 R H

TABLE 1.198 Compd. No.

k m n chirality R³

2168

1 2 0 R H

2169

1 2 0 R H

2170

1 2 0 R H

2171

1 2 0 R H

2172

1 2 0 R H

2173

1 2 0 R H

2174

1 2 0 R H

2175

1 2 0 R H

2176

1 2 0 R H

2177

1 2 0 R H

2178

1 2 0 R H

TABLE 1.199 Compd. No.

k m n chirality R³

2179

1 2 0 R H

2180

1 2 0 R H

2181

1 2 0 R H

2182

1 2 0 R H

2183

1 2 0 R H

2184

2 2 1 — H

2185

2 2 1 — H

2186

2 2 1 — H

2187

1 2 0 R H

2188

2 2 1 — H

2189

1 2 0 R H

TABLE 1.200 Compd. No.

k m n chirality R³

2190

2 2 1 — H

2191

2 2 1 — H

2192

2 2 1 — H

2193

2 2 1 — H

2194

2 2 1 — H

2195

2 2 1 — H

2196

1 2 0 R H

2197

1 2 0 R H

2198

1 2 0 R H

2199

2 2 1 — H

2200

2 2 1 — H

TABLE 1.201 Compd. No.

k m n chirality R³

2201

2 2 1 — H

2202

1 2 0 R H

2203

2 2 1 — H

2204

2 2 1 — H

2205

2 2 1 — H

2206

2 2 1 — H

2207

2 2 1 — H

2208

2 2 1 — H

2209

2 2 1 — H

2210

1 2 0 R H

2211

2 2 1 — H

TABLE 1.202 Compd. No.

k m n chirality R³

2212

2 2 1 — H

2213

2 2 1 — H

2214

2 2 1 — H

2215

1 2 0 R H

2216

1 2 0 R H

2217

1 2 0 R H

2218

1 2 0 R H

2219

1 2 0 R H

2220

1 2 0 R H

2221

1 2 0 R H

2222

1 2 0 R H

TABLE 1.203 Compd. No.

k m n chirality R³

2223

1 2 0 R H

2224

1 2 0 R H

2225

1 2 0 R H

2226

1 2 0 R H

2227

1 2 0 R H

2228

1 2 0 R H

2229

1 2 0 R H

2230

1 2 0 R H

2231

1 2 0 R H

2232

1 2 0 R H

2233

1 2 0 R H

TABLE 1.204 Compd. No.

k m n chirality R³

2234

1 2 0 R H

2235

1 2 0 R H

2236

1 2 0 R H

2237

1 2 0 R H

2238

1 2 0 R H

2239

1 2 0 R H

2240

1 2 0 R H

2241

1 2 0 R H

2242

1 2 0 R H

2243

1 2 0 R H

2244

1 2 0 R H

TABLE 1.205 Compd. No.

k m n chirality R³

2245

1 2 0 R H

2246

1 2 0 R H

2247

1 2 0 R H

2248

1 2 0 R H

2249

1 2 0 R H

2250

1 2 0 R H

2251

1 2 0 R H

2252

2 2 1 — H

2253

2 2 1 — H

2254

2 2 1 — H

2255

2 2 1 — H

TABLE 1.206 Compd. No.

k m n chirality R³

2256

2 2 1 — H

2257

2 2 1 — H

2258

1 2 0 R H

2259

1 2 0 R H

2260

1 2 0 R H

2261

1 2 0 R H

2262

1 2 0 R H

2263

1 2 0 S H

2264

1 2 0 S H

2265

1 2 0 S H

2266

1 2 0 S H

TABLE 1.207 Compd. No.

k m n chirality R³

2267

2 2 1 - H

2268

2 2 1 - H

2269

2 2 1 - H

2270

2 2 1 - H

2271

2 2 1 - H

2272

2 2 1 - H

2273

2 2 1 - H

2274

2 2 1 - H

2275

2 2 1 - H

2276

2 2 1 - H

2277

2 2 1 - H

TABLE 1.208 Compd. No.

k m n chirality R³

2278

1 2 0 R H

2279

1 2 0 R H

2280

1 2 0 S H

2281

1 2 0 S H

2282

2 2 1 - H

2283

2 2 1 - H

2284

2 2 1 - H

2285

2 2 1 - H

2286

2 2 1 - H

2287

2 2 1 - H

2288

2 2 1 - H

TABLE 1.209 Compd. No.

k m n chirality R³

2289

2 2 1 - H

2290

2 2 1 - H

2291

2 2 1 - H

2292

2 2 1 - H

2293

2 2 1 - H

2294

2 2 1 - H

2295

2 2 1 - H

2296

1 2 0 R H

2297

1 2 0 R H

2298

1 2 0 R H

2299

1 2 0 R H

TABLE 1.210 Compd. No.

k m n chirality R³

2300

1 2 0 S H

2301

1 2 0 S H

2302

1 2 0 R H

2303

1 2 0 R H

2304

1 2 0 R H

2305

1 2 0 S H

2306

1 2 0 S H

2307

1 2 0 R H

2308

1 2 0 R H

2309

1 2 0 S H

2310

1 2 0 S H

TABLE 1.211 Compd. No.

k m n chirality R³

2311

1 2 0 S H

2312

1 2 0 R H

2313

1 2 0 R H

2314

1 2 0 S H

2315

2 2 1 - H

2316

1 2 0 S H

2317

2 2 1 - H

2318

1 2 0 R H

2319

2 2 1 - H

2320

2 2 1 - H

2321

2 2 1 - H

TABLE 1.212 Compd. No.

k m n chirality R³

2322

2 2 1 - H

2323

2 2 1 - H

2324

2 2 1 - H

2325

1 2 0 R H

2326

1 2 0 R H

2327

1 2 0 S H

2328

1 2 0 S H

2329

1 2 0 S H

2330

1 2 0 S H

2331

1 2 0 S H

2332

1 2 0 R H

TABLE 1.213 Compd. No.

k m n chirality R³

2333

1 2 0 R H

2334

1 2 0 S H

2335

1 2 0 S H

2336

1 2 0 S H

2337

1 2 0 S H

2338

2 2 1 - H

2339

2 2 1 - H

2340

2 2 1 - H

2341

2 2 1 - H

2342

2 2 1 - H

2343

2 2 1 - H

TABLE 1.214 Compd. No.

k m n chirality R³

2344

2 2 1 - H

2345

2 2 1 - H

2346

2 2 1 - H

2347

1 2 0 S H

2348

1 2 0 R H

2349

1 2 0 R H

2350

1 2 0 R H

2351

1 2 0 R H

2352

2 2 1 - H

2353

2 2 1 - H

2354

1 2 0 R H

TABLE 1.215 Compd. No.

k m n chirality R³

2344

1 2 0 R H

2345

1 2 0 R H

2346

1 2 0 R H

2347

1 2 0 R H

2348

1 2 0 R H

2349

1 2 0 R H

2350

1 2 0 R H

2351

1 2 0 R H

2352

2 2 1 - H

2353

2 2 1 - H

2354

2 2 1 - H

TABLE 1.216 Compd. No.

k m n chirality R³

2366

2 2 1 - H

2367

2 2 1 - H

2368

2 2 1 - H

2369

2 2 1 - H

2370

2 2 1 - H

2371

2 2 1 - H

2372

2 2 1 - H

2373

2 2 1 - H

2374

2 2 1 - H

2375

2 2 1 - H

2376

2 2 1 - H

TABLE 1.217 Compd. No.

k m n chirality R³

2377

2 2 1 - H

2378

2 2 1 - H

2379

2 2 1 - H

2380

2 2 1 - H

2381

2 2 1 - H

2382

2 2 1 - H

2383

2 2 1 - H

2384

1 2 0 R H

2385

1 2 0 R H

2386

1 2 0 R H

2387

1 2 0 R H

TABLE 1.218 Compd. No.

k m n chirality R³

2388

1 2 0 R H

2389

1 2 0 R H

2390

1 2 0 R H

2391

1 2 0 R H

2392

1 2 0 R H

2393

1 2 0 R H

2394

2 2 1 - H

2395

2 2 1 - H

2396

2 2 1 - H

2397

2 2 1 - H

2398

2 2 1 - H

TABLE 1.219 Compd. No.

k m n chirality R³

2399

2 2 1 - H

2400

2 2 1 - H

2401

2 2 1 - H

2402

2 2 1 - H

2403

2 2 1 - H

2404

2 2 1 - H

2405

2 2 1 - H

2406

2 2 1 - H

2407

2 2 1 - H

2408

2 2 1 - H

2409

2 2 1 - H

TABLE 1.220 Compd. No.

k m n chirality R³

2410

2 2 1 - H

2411

2 2 1 - H

2412

2 2 1 - H

2413

2 2 1 - H

2414

2 2 1 - H

2415

2 2 1 - H

2416

2 2 1 - H

2417

2 2 1 - H

2418

2 2 1 - H

2419

2 2 1 - H

2420

2 2 1 - H

TABLE 1.221 Compd. No.

k m n chirality R³

2421

2 2 1 - H

2422

1 2 0 R H

2423

1 2 0 R H

2424

1 2 0 R H

2425

1 2 0 R H

2426

1 2 0 R H

2427

1 2 0 R H

2428

1 2 0 R H

In the present invention, the acid addition salt of the cyclic amine compound is also used. The acid includes mineral acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, and carbonic acid and organic acids such as maleic acid, citric acid, malic acid, tartaric acid, fumaric acid, methanesulfonic acid, trifluoroacetic acid and formic acid.

Further, the C₁ to C₆ alkyl addition salt of the cyclic amine compound such as 1-(4-chlorobenzyl)-1-methyl-4-[{N-(3-trifluoromethylbenzoyl)glycyl} aminomethyl]piperidinium iodide is also used in the present invention. The alkyl group includes a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, an n-hexyl group, an n-heptyl group, an n-octyl group, an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a 2-methylpentyl group and a 1-ethylbutyl group as suitable examples, but includes the methyl group and the ethyl group as especially preferable concrete examples. The counter anion of the ammonium cation includes halide anions such as a fluoride ion, a chloride ion, a bromide ion and an iodide ion as suitable concrete examples.

In the present invention, the racemate and all the possible optical isomers of the compound represented by the formula (I) can be used.

The compound represented by the formula (I) can be synthesized by either of the following general preparation methods, as mentioned in WO 99/25686.

(Preparation Method 1)

A preparation method by reacting 1 equivalent of a compound represented by the following formula (II)

[wherein, R¹, R², R³, j, k, m, and n are the same as the definitions, respectively, in the above-described formula (I)], with 0.1 to 10 equivalents of a carboxylic acid represented by the following formula (III) or a reactive derivative thereof

[wherein, R⁴, R⁵, R⁶, G, p, and q are the same as the definitions, respectively, in the above-mentioned formula (I)], in the absence or presence of a solvent.

“The reactive derivative” of the carboxylic acid represented by the above-mentioned formula (III) means a highly reactive carboxylic acid derivative usually used in the field of synthetic organic chemistry, such as an acid halide, an acid anhydride, a mixed acid anhydride or the like.

The reaction can be allowed to smoothly proceed by the suitable use of proper amounts of a dehydrating agent, such as molecular sieve; a coupling reagent such as dicyclohexylcarbodiimide (DCC), N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide (EDCI or WSC), carbonyldiimidazole (CDI), N-hydroxysuccinimide (HOSu), N-hydroxybenzotriazole (HOBt), benzotriazol-1-yloxytris(pyrrolidino)phosphonium hexafluorophosphate (PyBOP), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramthyluronium hexafluorophosphate (HBTU), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU), 2-(5-norbornene-2,3-dicarboxyimido)-1,1,3,3-tetramethyluronium tetrafluoroborate (TNTU), O-(N-succinimidyl)-1,1,3,3-tetramethyluronium tetrafluorbborate (TST-U) or bromotris(pyrrolidino)phosphonium hexafluorophosphate (PyBroP); and a base, for example, an inorganic base such as potassium carbonate, calcium carbonate or sodium bicarbonate, an amine such as triethylamine, diisopropylethylamine or pyridine, or a polymer supported base such as (piperidinomethyl)polystyrene, (morpholinomethyl)polystyrene, (dimethylaminomethyl)polystyrene, poly(4-vinylpyridine) or the like.

(Preparation Method 2)

A preparation method by reacting 1 equivalent of an alkylating reagent represented by the following formula (IV)

[wherein, R¹, R², and j are the same as the definitions, respectively, in the above-described formula (I); X represents a halogen atom, an alkylsulfonyloxy group, or an arylsulfonyloxy group], with 0.1 to 10 equivalents of a compound represented by the following formula (V)

[wherein, R³, R⁴, R⁵, R⁶, G, k, m, n, p, and q are the same as the definitions, respectively, in the above-mentioned formula (I)], in the absence or presence of a solvent.

The reaction can be allowed to smoothly proceed by the suitable use of the same base as that in the above-mentioned preparation method 1. Further, in the present preparation method, the reaction can be accelerated by the coexistence of an iodide compound such as potassium iodide, sodium iodide or the like in some cases.

In the above-mentioned formula (IV), X represents a halogen atom, an alkylsulfonyloxy group or an arylsulfonyloxy group. The suitable examples of the halogen atoms include a chlorine atom, a bromine atom, and an iodine atom. The suitable concrete example of the alkylsulfonyloxy group includes a methylsulfonyloxy group, a trifluoromethylsulfonyloxy group and the like. The suitable concrete example of the arylsulfonyloxy group includes a tosyloxy group.

(Preparation Method 3)

A preparation method by reacting 1 equivalent of an aldehyde represented by the following formula (VI)

[wherein, R¹, and R² are the same as the definitions, respectively, in the above-mentioned formula (I); j represents 1 or 2], or the following formula (VII) R¹—CHO  (VII) [wherein, R¹ is the same as the definition in the above-mentioned formula (I); this compound corresponds to a case that j expresses 0 in the formula (I)] with 0.1 to 10 equivalents of a compound represented by the above-mentioned formula (V), in the absence or presence of a solvent.

The reaction is generally called a reductive amination reaction, and includes, as a reducing condition, a catalytic hydrogenation reaction using a catalyst containing a metal such as palladium, platinum, nickel or rhodium, a hydrogenation reaction using a borane or a complex hydride such as lithium aluminum hydride, sodium borohydride, sodium cyanoborohydride, or sodium triacetoxyborohydride and an electrolytic reduction reaction.

(Preparation Method 4)

A preparation method by reacting 1 equivalent of a compound represented by the following formula (VIII)

[wherein, R¹, R², R³, R⁴, R⁵, R⁷, j, k, m, n, p, and q are the same as the definitions, respectively, in the above-mentioned formula (I)], with 0.1 to 10 equivalents of a carboxylic acid or sulfonic acid represented by the following formula (IX) or a reactive derivative thereof HO—A—R⁶  (IX) [wherein, R⁶ is the same as the definition of R⁶ in the above-mentioned formula (I); “A” represents a carbonyl group or a sulfonyl group], in the absence or presence of a solvent.

The reactive derivative of the carboxylic acid or sulfonic acid represented by the formula (IX) means a highly reactive carboxylic acid or sulfonic acid derivative generally used in the field of synthetic organic chemistry, such as an acid halide, an acid anhydride or a mixed acid anhydride.

The reaction can be allowed to smoothly proceed by the suitable use of the same dehydrating agent, coupling reagent or base as those in the above-mentioned preparation method 1.

(Preparation Method 5)

A preparation method by reacting 1 equivalent of a compound represented by the above-mentioned formula (VIII) with 0.1 to 10 equivalents of an isocyanate or isothiocyanate represented by the following formula (X) Z═C═N—R⁶  (X) [wherein, R⁶ is the same as the definition of R⁶ in the above-mentioned formula (I); Z represents an oxygen atom or a sulfur atom], in the absence or presence of a solvent. (Preparation Method 6)

A preparation method by reacting 1 equivalent of a compound represented by the following formula (XI)

[wherein, R¹, R², R³, R⁴, R⁵, j, k, m, n, p, and q are the same as the definitions, respectively, in the above-mentioned formula (I); “A” represents a carbonyl group or a sulfonyl group], with 0.1 to 10 equivalents of an amine represented by the following formula (XII) R⁶—NH₂  (XII) [wherein, R⁶ is the same as the definition of R⁶ in the above-mentioned formula (I)], in the absence or presence of a solvent.

The reaction can be allowed to smoothly proceed by the suitable use of the same dehydrating agent, coupling reagent or base as those in the above-mentioned preparation method 1.

When the substrate supplied for the reaction in each of the above-mentioned preparation methods 1 to 6 has substituents which can be thought to generally react under the reaction conditions of each preparation method in organic synthetic chemistry or affect the reaction, the objective compound can be obtained by protecting the functional groups of the substrate with known proper protecting groups, supplying the protected substrate for the reaction and then removing the protecting groups by a known method.

In addition, the compound used in the present invention can also be obtained by further converting the (single or plural) substituent(s) of the compound prepared by the above-mentioned preparation method 1 to 6 by a known reaction generally used in organic synthetic chemistry, such as an alkylation reaction, an acylation reaction or a reduction reaction.

In each of the above-mentioned preparation methods, a halogenated hydrocarbon such as dichloromethane or chloroform, an aromatic hydrocarbon such as benzene or toluene, an ether such as diethyl ether or tetrahydrofuran, an ester such as ethyl acetate, an aprotic polar solvent such as dimethyl formamide, dimethyl sulfoxide or acetonitrile, or an alcohol such as methanol, ethanol or isopropyl alcohol, is suitably used as a reaction solvent in response to the reaction.

In any preparation method, the reaction temperature is in the range of −78° C. to +150° C., preferably 0° C. to 100° C. After the reaction is completed, the objective cyclic amine compound represented by the above-mentioned formula (I) can be isolated in usual isolating and purifying operations, namely the operations of concentration, filtration, extraction, solid-phase extraction, recrystallization, chromatography, and so on. Further, the isolated compound can be converted into a pharmaceutically acceptable acid addition salt or C₁ to C₆ alkyl addition salt by usual methods.

EXAMPLES

The present invention will be explained specifically hereafter on the basis of examples. However, the present invention is not limited to the examples. Compound numbers assigned to compounds in the following examples correspond to compound numbers (Compd. No.), respectively, assigned to compounds shown as suitable concrete examples in Tables 1.1 to 1.221.

Reference Example 1 Synthesis of (R)-1-(4-chlorobenzyl)-3-[{N-(3,4-difluorobenzoyl) glycyl}amino]pyrrolidine (Compd. No. 69)

The compounds of the present invention were synthesized by the preparation method mentioned in WO 99/25686, and, for example, (R)-1-(4-chlorobenzyl)-3-[{N-(3,4-difluorobenzoyl)glycyl}amino]pyrrolidine of Compd. No. 69 was synthesized as follows.

1) 3-Amino-1-(4-chlorobenzyl)pyrrolidine-dihydrochloride

4-Chlorobenzyl chloride (4.15 g, 25.8 mmol) and i-Pr₂NEt (6.67 g, 51.6 mmol) were added to the DMF solution (50 mL of 3-{(tert-butoxycarbonyl)amino}pyrrolidine (4.81 g, 25.8 mmol) in DMF (50 ml). The reaction mixture was stirred at 70° C. for 15 hours, and the solvent was then removed under reduced pressure. The residue was recrystallized (CH₃CN, 50 mL) to obtain the objective 3-{(tert-butoxycarbonyl)amino}-1-(4-chlorobenzyl)pyrrolidine (6.43 g, 80%) as the yellowish white solid.

¹H-NMR (CDCl₃, 300 MHz) δ 1.37 (s, 9H), 1.5-1.7 (br, 1H), 2.1-2.4 (m, 2H), 2.5-2.7 (m, 2H), 2.83 (br, 1H), 3.57 (s, 2H), 4.1-4.3 (br, 1H), 4.9-5.1 (br, 1H), 7.15-7.35 (br, 4H); the purity was determined with RPLC/MS (98%); ESI/MS m/e 311.0 (M⁺+H, C₁₆H₂₄ClN₂O₂).

1M HCl-Et₂O (100 mL) was added to the CH₃OH (80 mL) solution of the 3-{(tert-butoxycarbonyl)amino}-1-(4-chlorobenzyl)pyrrolidine (6.38 g, 20.5 mmol) and then stirred at 25° C. for 15 hours. The solvent was removed under reduced pressure to obtain the solid. The solid was recrystallized (CH₃OH/CH₃CN=1:2, 130 mL) to obtain the purified 3-amino-1-(4-chlorobenzyl)pyrrolidine·dihydrochloride (4.939 g, 85%) as white powder.

¹H-NMR (d₆-DMSO, 300 MHz) δ 3.15 (br, 1H), 3.3-3.75 (br-m, 4H), 3.9 (br, 1H), 4.05 (br, 1H), 4.44 (br, 1H), 4.54 (br, 1H), 7.5-7.7 (m, 4H), 8.45 (br, 1H), 8.60 (br, 1H); the purity was determined with RPLC/MS (>99%); ESI/MS m/e 211.0 (M⁺+H, C₁₁H₁₆ClN₂).

Optically active (R)-3-amino-1-(4-chlorobenzyl)pyrrolidine-dihydrochloride and (S)-3-amino-1-(4-chlorobenzyl)pyrrolidine-dihydrochloride were synthesized from the corresponding starting materials, respectively, by the above-mentioned method. The products showed the same ¹H-NMR as that of the above-mentioned racemate.

2) (R)-3-{(N-tert-βutoxycarbonyl)glycyl}amino-1-(4-chlorobenzyl)pyrrolidine

A mixture of (R)-3-amino-1-(4-chlorobenzyl)pyrrolidine-dihydrochloride (4.54 g, 16.0 mmol), a 2M NaOH solution (80 mL), and ethyl acetate (80 mL) was stirred, and the organic layer was then separated. The aqueous layer was extracted with ethyl acetate (80 mL×2). The obtained organic layers were combined, dried over anhydrous sodium sulfate, filtered, and then concentrated to obtain the free (R)-3-amino-1-(4-chlorobenzyl)pyrrolidine (3.35 g, 99%).

Et₃N (2.5 mL, 17.6 mmol), N-tert-butoxycarbonylglycine (2.79 g, 16.0 mmol), EDCI (3.07 g, 16.0 mmol) and HOBt (12.16 g, 16 mmol) were added to the CH₂Cl₂ (80 mL) solution of the (R)-3-amino-1-(4-chlorobenzyl)pyrrolidine (3.35 g, 16 mmol). The reaction mixture was stirred at 25° C. for 16 hours, and then mixed with a 2M NaOH solution (80 mL). The organic layer was separated, and the aqueous layer was extracted with dichloromethane (100 mL×3). The obtained organic layers were combined, washed with water (100 mL×2) and aqueous sodium chloride solution (100 mL), dried over anhydrous sodium sulfate, filtered and then concentrated. The objective (R)-3-{N-(tert-butoxycarbonyl)glycyl}amino-1-(4-chlorobenzyl)pyrrolidine (5.40 g, 92%) was obtained by column chromatography (SiO₂, ethyl acetate).

3) Synthesis of (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine

A 4M HCl dioxane (38 mL) solution was added to the methanol (60 mL) solution of the (R)-3-{N-(tert-butoxycarbonyl)glycyl}amino-1-(4-chlorobenzyl)pyrrolidine (5.39 g, 14.7 mmol). The solution was stirred at room temperature for 2 hours. The reaction mixture was concentrated and then mixed with a 2M NaOH solution (80 mL). The mixture was extracted with dichloromethane (80 mL×3), and the extracts were combined, dried over anhydrous sodium sulfate, and then concentrated. The (R)-3-(glycylamino)-1-(4-chlorobenzyl)pyrrolidine (3.374 g, 86%) was obtained by column chromatography (SiO₂, AcOEt/EtOH/Et₃N=90/5/5).

¹H-NMR (CDCl₃, 270 MHz) δ 1.77 (dd, J=1.3 and 6.9 Hz, 1H), 2.20-3.39 (m, 2H), 2.53 (dd, J=3.3 and 9.6 Hz, 1H), 2.62 (dd, J=6.6 and 9.6 Hz, 1H), 2.78-2.87 (m, 1H), 3.31 (s, 2H), 3.57 (s, 2H), 4.38-4.53 (br, 1H), 7.18-7.32 (m, 4H), 7.39 (br, s, 1H).

4) (R)-1-(4-Chlorobenzyl)-3-[{N-(3,4-difluorobenzoyl)glycyl}amino]pyrrolidine (Compd. No. 69)

The chloroform (0.4 mL) solution of 3,4-difluorobenzoyl chloride (0.060 mmol) was added to the chloroform (1.0 mL) solution of the (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine (0.050 mmol) and triethylamine (0.070 mmol). The reaction mixture was stirred at room temperature for 2.5 hours, and then mixed with a (aminomethyl)polystyrene resin (1.04 mmol/g, 50 mg, 50 mmol). The mixture was stirred at room temperature for 12 hours, and filtered. The resin was washed with dichloromethane (0.5 mL). The filtrate and the washings were combined and mixed with dichloromethane (4 mL). The solution was washed with a 2M NaOH aqueous solution (0.5 mL), and then concentrated to obtain the (R)-1-(4-chlorobenzyl)-3-[{N-(3,4-difluorobenzoyl)glycyl}amino]pyrrolidine (Compd. No. 69) (7.8 mg, 38%): the purity was determined with RPLC/MS (>99%); ESI/MS m/e 408.0 (M⁺+H, C₂₀H₂₀ClF₂N₃O₂).

Example 1 Assay of the Inhibitory Potency of a Compound Against the Rise in the Intracellular Calcium Concentration of CCR3 Expressing Cells by Eotaxin

The inhibitory potency of the compound of the present invention against the rise in the intracellular calcium concentration was assayed using K562 cells stably expressing a CCR3 receptor by the following method.

A 1 mM Fura 2 acetoxymethyl ester (Dojin Kagaku Co.) was added to a suspension obtained by suspending the CCR3 expressing K562 cells in a 10 mM HEPES-containing HBSS solution, and then incubated at 37° C. for 30 minutes. The suspension was excited with 340 nm and 380 nm light, and the 340/380 ratio was monitored to measure the intracellular calcium concentration. Human eotaxin (0.5 μg/ml) was used as an agonist, and the inhibitory potency of the compound was assayed by treating the CCR3 expressing K562 cells with the compound at five minutes before the stimulation using the eotaxin, assaying the intracellular calcium concentration of the treated CCR3 expressing K562 cells, and then calculating the inhibition potency (%) by the use of the following expression. Inhibition rate (%)={1−(A−B)/(C−B)}×100 (A: an intracellular calcium concentration, when the cells were treated with the compound and then stimulated with the eotaxin; B: an intracellular calcium concentration, when the cells were not stimulated with the eotaxin; C: an intracellular calcium concentration, when the cells were not treated with the compound but stimulated with the eotaxin).

When the inhibitory activities of the cyclic amine derivatives used in the present invention were assayed, for example, the following compounds showed inhibitory activities of 20% to 50%, 50% to 80%, and >80%, respectively, at a concentration of 10 μM.

The compounds which showed the inhibitory activities of 20% to 50% at the concentration of 10 μM:

Compd. Nos. 11, 156, 234, 330, 392, 424, 481, 523, 525, 533, 558, 567, 582, 602, 613, 630, 646, 649, 701, 738, 741, 754, 767, 814, 816, 833, 839, 873, 902, 909, 945, 1002, 1159, 1170, 1258, 1315, 1352, 1357, 1407, 1417, 1448, 1472, 1504, 1508, 1531, 1558, 1562, 1569, 1661, 1670, 1686, 1719, 1751, 1756, 1769, 1775, 1783, 1797, 1802, 1803, 1815, 1834, 1841, 1846, 1883, 1887, 1889, 1892, 1913, 1924, 1928, 1960, 2006, 2013, 2035, 2052, 2083, 2113, 2127, 2136, 2189, 2320, 2321, 2323, 2327, 2330, 2334, 2336, 2338, 2345, 2394, 2394, 2398, 2398, 2400, 2400, 2406, 2406, 2407, 2407, 2409, 2409, 2420, 2420, 2421, 2421

The compounds which showed the inhibitory activities of 50% to 80% at the concentration of 10 μL M:

Compd. Nos. 83, 115, 146, 150, 216, 294, 297, 322, 405, 440, 459, 461, 466, 482, 484, 487, 490, 492, 503, 526, 528, 550, 562, 570, 578, 620, 623, 659, 685, 687, 703, 716, 730, 733, 755, 770, 850, 856, 867, 876, 998, 1015, 1024, 1223, 1259, 1267, 1295, 1377, 1402, 1412, 1420, 1485, 1519, 1550, 1560, 1595, 1601, 1650, 1701, 1725, 1754, 1836, 1856, 1870, 1912, 1923, 1929, 2095, 2120, 2138, 2179, 2258, 2260, 2261, 2267, 2268, 2270, 2275, 2276, 2278, 2287, 2290, 2291, 2294, 2297, 2300, 2301, 2302, 2307, 2309, 2313, 2317, 2322, 2324, 2326, 2328, 2329, 2333, 2335, 2343, 2344, 2346, 2347, 2348, 2350, 2351, 2353, 2358, 2360, 2361, 2364, 2365, 2368, 2369, 2377, 2379, 2381, 2402, 2403, 2404, 2405, 2408, 2410, 2411, 2416, 2417, 2418

The compounds which showed the inhibitory activities of >80% at the concentration of 10 μM:

Compd. Nos. 7, 32, 68, 169, 173, 203, 209, 215, 520, 544, 547, 851, 852, 855, 874, 910, 1003, 1012, 1032, 1038, 1042, 1043, 1046, 1114, 1190, 1244, 1247, 1384, 1441, 1513, 1527, 1545, 1582, 1673, 1687, 1689, 1705, 1850, 1869, 1871, 1876, 1877, 1899, 2027, 2289, 2293, 2296, 2298, 2315, 2318, 2319, 2325, 2332, 2349, 2352, 2354, 2355, 2356, 2357, 2359, 2362, 2363, 2366, 2367, 2370, 2371, 2372, 2373, 2374, 2375, 2376, 2378, 2382, 2383, 2390, 2393, 2396, 2412, 2413, 2414, 2415, 2422, 2423, 2424, 2425, 2426, 2427, 2428

Example 2 Assay of Inhibitory Potency Against the Binding of Eotaxin to a CCR3 Expressing Cells Membrane Fraction

A cell membrane fraction prepared from human CCR3 expressing K562 cells was suspended in an assay buffer solution (25 mM HEPES, pH 7.6, 1 mM CaCl₂, 5 mM MgCl₂, 0.5% BSA) at a concentration of 0.5 mg/mL to prepare the cell membrane fraction suspension. A test compound was diluted with the assay buffer solution to prepare the test compound solution. [¹²⁵I]-labeled human eotaxin (Amasham Co.) was diluted with the assay buffer solution at a concentration of 1 μCi/mL to prepare the labeled ligand solution. 25 μL of the test compound solution, 25 μL of the labeled ligand solution and 50 μL of the cell membrane fraction suspension were sequentially injected into each well of a 96 well microplate coated with 0.5% BSA, stirred (100 μL of the reaction solution), and then incubated at 25° C. for 90 minutes.

After the reaction was finished, the reaction solution was filtered with the 96 well filter plate (Millipore Inc.) in which the filter was previously immersed in a 0.5% polyethylenimine solution, and the filter was washed with 150 μL of a cold washing buffer solution (assay buffer+0.5M NaCl) four times (150 μL of the cold washing buffer solution was added and then filtered). After the filter was dried with air, 25 μL of a liquid scintillator was added to each well, and the radioactivity retained in the membrane fraction on the filter was measured with a TopCounter (Packard Co.).

The inhibitory potency of the test compound against the binding of the human eotaxin to the CCR3 membrane fraction was calculated, wherein a count on the addition of 100 ng of non-labeled human eotaxin in stead of the test compound was subtracted, and a count on the non-addition of the test compound was 100%. Inhibition (%)={1−(A−B)/(C−B)}×100 (A: a count, when the test compound was added; B: a count, when 100 ng of the non-labeled human eotaxin was added; C: a count, when only [¹²⁵I]-labeled human eotaxin was added).

When the inhibitory activities of the cyclic amine derivatives used in the present invention were assayed, the inhibitory activities of typical compounds in the present example were approximately equivalent to the inhibitory activities measured in Example 1.

UTILIZABILITY IN INDUSTRY

The medicine containing as an active ingredient the cyclic amine compound, the pharmaceutically acceptable acid addition salt thereof or the pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof, of the present invention, or the medicine for treating or preventing diseases in which CCR3 participates, has an activity for inhibiting the action of the ligand of the CCR3, such as eotaxin, to a target cell as the CCR3 antagonist. Thereby, the medicine is useful as a medicine for treating and/or preventing diseases for whose progress and maintenance the tissue infiltration of eosinophils, basophils, activated T-cells and so on play main rolls, for example, allergic diseases such as bronchial asthma, allergic rhinitis, atopic dermatitis, urticaria, contact dermatitis and allergic conjunctivitis, inflammatory bowel diseases such as ulcerative colitis, Crohn disease and so on. Further, the medicine is useful as a medicine for treating and/or preventing AIDS by the HIV-1 infection-inhibiting activity based on the CCR3 antagonism. 

1. A method for treatment of allergic conjunctivitis, eosinophilia, eosinophilic gastroentereitis, eosinophilic enteropathy, eosinophilic fasciitis, eosinophilic granuloma, eosinophilic pustular folliculitis, and eosinophilic leukemia, comprising administering to a subject an effective amount of a compound having CCR3 antagonistic activity, wherein said compound is represented by the following formula (I), a pharmaceutically acceptable acid addition salt thereof, or a pharmaceutically acceptable C₁ to C₆ alkyl addition salt thereof,

wherein, R¹ represents an aromatic heterocyclic group selected from the group consisting of an imidazolyl group, a pyrazolyl group, an oxazolyl group, an isoxazolyl group, a thiazolyl group, an isothiazolyl group, a pyrimidinyl group, a triazinyl group, a triazolyl group, an oxadiazolyl group, a thiadiazolyl group, a thienothienyl group, an indolyl group, a benzofuranyl group a benzothienyl group, a quinolyl group, a benzimidazolyl group, a benzoxazolyl group, a benzotriazolyl group, a benzoxadiazolyl group, a benzothiadiazolyl group, further provided that the naphthyl group or the aromatic heterocyclic group may be substituted by one or more halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, C₁ to C₆ alkyl groups, C₃ to C₈ cycloalkyl groups, C₂ to C₆ alkenyl groups, C1 to C6 alkoxy groups, C₁ to C₆ alkylthio groups, C₃ to C₅ alkylene groups, C₂ to C₄ alkylenoxy groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylthio groups, benzyl groups, benzyloxy groups, benzoylamino groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₄ to C₉ N-cycloalkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, C₃ to C₈ (alkoxycarbonyl)methyl groups, N-phenylcarbamoyl groups, piperidinocarbonyl groups, morpholinocarbonyl groups, 1-pyrrolidinylcarbonyl groups, divalent groups represented by the formula: —NH(C═O)O—, divalent groups represented by the formula: —NH(C═S)O—, amino groups, mono(C₁ to C₆ alkyl)amino groups or di(C₁ to C₆ alkyl)amino groups, and further provided that the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the aromatic heterocyclic group or the condensed ring may further be substituted by one or more halogen atoms, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups; R² represents a hydrogen atom, a C₁ to C₆ alkyl group, a C₂ to C₇ alkoxycarbonyl group, a hydroxy group or a phenyl group, provided that the C₁ to C₆ alkyl group or the phenyl group in R² may be substituted by one or more halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups, and provided that when j is 0, R² is not a hydroxy group; j is 0; k represents 0 or 1; m represents an integer of 2 to 3; n represents 0; R³ represents a hydrogen atom or a C₁ to C₆ alkyl group which may be substituted by one or two phenyl groups which may be substituted by the same or different numbers of halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups or C₁ to C₆ alkoxy groups; R⁴ and R⁵, which may be the same or different, represent a hydrogen atom, a hydroxy group, a phenyl group or a C₁ to C₆ alkyl group, and the C₁ to C₆ alkyl group represented by R⁴ and/or R⁵ may be substituted by one or more halogen atoms, hydroxy groups, cyano groups, nitro groups, carboxyl groups, carbamoyl groups, mercapto groups, guanidino groups, C₃ to C₈ cycloalkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, phenyl groups which may be substituted by one or more halogen atoms, hydroxy groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups or benzyloxy groups, phenoxy groups, benzyloxy groups, benzyloxycarbonyl groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino groups, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, amino groups, mono(C₁ to C₆ alkyl)amino groups, di(C₁ to C₆ alkyl)amino groups or aromatic heterocyclic groups (having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms), or condensed rings formed by the condensation of the aromatic heterocyclic group with a benzene ring, or R⁴ and R⁵ may together form a three to six-membered cyclic hydrocarbon; p represents 0 or 1; q represents 0 or 1; G represents a group represented by —NR⁷—CO—, —NH—CO—NH—, or —NH—CS—NH provided that R⁷ is a hydrogen atom; R⁶ represents a phenyl group, a C₃ to C₈ cycloalkyl group, a C₃ to C₆ cycloalkenyl group, a benzyl group or an aromatic heterocyclic group having one to three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, provided that the phenyl group, the benzyl group or the aromatic heterocyclic group represented by R⁶ may be condensed, to make a condensed ring, with a benzene ring or an aromatic heterocyclic group having one or three atoms of oxygen, sulfur and/or nitrogen as heteroatoms, further provided that the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₆ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group or the condensed ring represented by R⁶ may be substituted by one or more halogen atoms, hydroxy groups, mercapto groups, cyano groups, nitro groups, thiocyanato groups, carboxyl groups, carbamoyl groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₃ to C₆ cycloalkyl groups, C₂ to C₆ alkenyl groups, C₁ to C₆ alkoxy groups, C₃ to C₈ cycloalkyloxy groups, C₁ to C₆ alkylthio groups, C₁ to C₃ alkylenedioxy groups, phenyl groups, phenoxy groups, phenylamino groups, benzyl groups, benzoyl groups, phenylsulfinyl groups, phenylsulfonyl groups, 3-phenylureido groups, C₂ to C₇ alkanoyl groups, C₂ to C₇ alkoxycarbonyl groups, C₂ to C₇ alkanoyloxy groups, C₂ to C₇ alkanoylamino group, C₂ to C₇ N-alkylcarbamoyl groups, C₁ to C₆ alkylsulfonyl groups, phenylcarbamoyl groups, N,N-di(C₁ to C₆ alkyl)sulfamoyl groups, amino groups, mono(C₁ to C₆ alkyl)amino groups, di(C₁ to C₆ alkyl)amino groups, benzylamino groups, C₂ to C₇ (alkoxycarbonyl)amino groups, C₁ to C₆ (alkylsulfonyl)amino groups or bis(C₁ to C₆ alkylsulfonyl)amino groups, and further provided that the substituents of the phenyl group, the C₃ to C₈ cycloalkyl group, the C₃ to C₈ cycloalkenyl group, the benzyl group, the aromatic heterocyclic group, or the condensed ring may further be substituted by one or more halogen atoms, cyano groups, hydroxy groups, amino groups, trifluoromethyl groups, C₁ to C₆ alkyl groups, C₁ to C₆ alkoxy groups, C₁ to C₆ alkylthio groups, mono(C₁ to C₆ alkyl)amino groups, or di(C₁ to C₆ alkyl)amino groups; and wherein m+k is
 3. 2. The method according to claim 1, wherein k is 1 and m is 2 in said formula (I). 